| A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | AA | AB | AC | AD | AE | AF | AG | AH | AI | AJ | AK | AL | AM | AN | AO | AP | AQ | AR | AS | AT | AU | AV | AW | AX | AY | AZ | BA | BB | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | Deal Date | R&D | Licensor Category | Client | Licensee Category | Deal Types | Stages | Size ($M) | Upfront Cash ($M) | Deal Subject | Web Link | Deal ID | Primary Doc | Equity ($M) | Maximum Share (%) | Amendment Date | Termination Date | Contracts | PRs | Deal Source | Exclusivity | Diseases | Indications | Technologies | Sub Technologies | Territory | Sub-Territory | Compound Name | MOA Category | Mechanism of Action | Molecular Target | Drug Mode of Action | Upfront Equity ($M) | Contingent Equity ($M) | R&D Support ($M) | FTE Rate ($M) | Loan ($M) | Dev / Reg Milestones ($M) | Other Milestones ($M) | Total Precommercial Payments ($M) | Sales Milestones ($M) | Deal Size ($M) | Upfront Share (%) | Dev Share (%) | Sales Share (%) | EFR$200M (%) | EFR$500M (%) | EFR$1B (%) | Maximum Royalty (%) | Marketing Fee (%) | Transfer Price (%) | Manufacture Cost + (%) | Profit Split (%) | Financial Term Explanations |
2 | 06/2021 | AnHeart Therapeutics | Innovent Biologics | Co-Development, License, Supply | Phase II | 189.00 | Taletrectinib tyrosine kinase inhibitor targeting ROS1 and NTRK in Greater China | Link | 18709 | AnHeart_Innovent_060121.pdf | Yes | PR | Exclusive | Cancer | Lung, Solid Tumors | Synthetics | Small Molecule | Asia | China | taletrectinib, DS-6051 | Kinase | neurotrophic tyrosine kinase receptor 1 (NTRK1), c-ros proto-oncogene 1 receptor tyrosine kinase (ROS1) | Inhibitor | 189.00 | tiered royalties | upfront payment, R&D fees, and potential milestone payments totaling $189M | |||||||||||||||||||||||||||||
3 | 06/2021 | Arrowhead Pharmaceuticals | Horizon Therapeutics | License | Preclinical | 700.00 | 40.00 | ARO-XDH RNAi therapeutic targeting xanthine dehydrogenase to treat uncontrolled gout | Link | 18860 | Arrowhead_Horizon_062121.pdf | Yes | PR | Exclusive | Autoimmune/Inflammatory | Other Autoimmune/Inflammatory | Oligonucleotides | RNAi | Worldwide | 700.00 | 5.71 | Royalties ranging from the low- to mid-teens | $660M in development, regulatory and commercial milestones | ||||||||||||||||||||||||||||||||
4 | 06/2021 | Beam Therapeutics | 2013-21 IPOs | Apellis Pharmaceuticals | 2013-21 IPOs | Co-Development, Co-Promotion, Option, Research | Discovery | 75.00 | 75.00 | Base editing technology for up to six research programs focused on C3 and other complement targets | Link | 18944 | Beam_Apellis_063021.pdf | Yes | PR | Exclusive | Central Nervous System, Liver & Gallbladder Diseases, Ophthalmic | Broad Focus Central Nervous System, Broad Focus Liver & Gallbladder Diseases, Broad Focus Ophthalmic | 75.00 | 100.00 | $50M upon signing and additional $25M on one-year anniversary of the contract execution date | Undisclosed development, regulatory, and sales milestones | |||||||||||||||||||||||||||||||||
5 | 06/2021 | Bolt Biotherapeutics | 2013-21 IPOs | Genmab | 2013-21 IPOs | Co-Development, Equity, License, Option, Research | Discovery | 880.00 | 10.00 | Bispecific immune-stimulating antibody conjugates to treat cancer | Link | 18742 | Bolt_Genmab_060221.pdf | 15.00 | Yes | PR | Cancer | Broad Focus Cancer | Monoclonals | Bispecific, Conjugates | 15.00 | 880.00 | 2.84 | $285M in milestones per therapeutic candidate, Genmab has option to up to three therapeutic candidates | ||||||||||||||||||||||||||||||
6 | 06/2021 | Cyclerion | Akebia Therapeutics | 2013-21 IPOs | License | Phase II | 585.00 | Praliciguat oral sGC stimulator for renal indications | Link | 18732 | Cyclerion_Akebia_060421.pdf | Yes | PR | Exclusive | Renal | Synthetics | Small Molecule | Worldwide | 225.00 | 585.00 | 38.46 | Tiered royalties ranging from single-digit to high-teen percentages | $225M in pre-commercial milestones, including up to $15M in the first 18 months | Total potential future development, regulatory, and commercialization milestones up to $585M | ||||||||||||||||||||||||||||||||
7 | 06/2021 | Eisai | Top Pharma, Japanese Pharma | Bristol-Myers Squibb | Top Pharma | Co-Development, Co-Promotion, License, Supply | Phase I | 3,100.00 | 450.00 | MORAb-202 antibody drug conjugate for solid tumors | Link | 18842 | Eisai_BMS_061721.pdf | Yes | PR | Exclusive | Cancer | Solid Tumors | Monoclonals | Conjugates | Worldwide | eribulin/farletuzumab, MORAb-202 | folate receptor 1 (FOLR1) | Antagonist | 200.00 | 3,100.00 | 14.52 | $2.45 billion in development, regulatory, and commercial milestones | ||||||||||||||||||||||||||
8 | 06/2021 | Halozyme Therapeutics | ViiV Healthcare | License | Formulation | 740.00 | 40.00 | Enhanze drug delivery technology for subcutaneous formulation of four HIV drug targets | Link | 18862 | Halozyme_ViiV_062221.pdf | Yes | PR | Exclusive | Infectious-Viral | Human Immunodeficiency Virus/HIV | Drug Delivery, Recombinant DNA | Other | Worldwide | 740.00 | 5.41 | Mid-single digit royalties | Up to $175M in development and commercial milestones, including sales milestones, per target | ||||||||||||||||||||||||||||||||
9 | 06/2021 | Heartseed | Novo Nordisk | Top Pharma | Co-Promotion, License, Option | Preclinical | 598.00 | 55.00 | HS-001 iPSC-derived cell therapy to treat heart failure ex-Japan | Link | 18718 | Heartseed_NovoNordisk_060121.pdf | Yes | PR | Exclusive | Cardiovascular | Congestive Heart Failure | Cell Therapy - Stem Cells/Factors | Africa, Asia, Europe, Middle East, NAFTA, South America | All African Countries, All European Countries, All Middle East Countries, All NAFTA Countries, All South American Countries, Australia, China, India, New Zealand, Other Asian, Southeast Asia | 598.00 | 9.20 | Tiered high single-digit to low double-digit royalties | Payments totaling up to $598M including $55M in upfront and near-term milestone payments | |||||||||||||||||||||||||||||||
10 | 06/2021 | HiFiBiO | FibroGen | 2013-21 IPOs | License, Option | Preclinical | 1,125.00 | 25.00 | Galectin-9 program for cancer and autoimmune indications, option to CXCR5 and CCR8 programs | Link | 18845 | FibroGen_HiFiBiO_0621_Lic.pdf | Yes | Yes | SEC Redacted | Exclusive | Autoimmune/Inflammatory, Cancer | Broad Focus Autoimmune/Inflammatory, Broad Focus Cancer | Monoclonals | Worldwide | 1,125.00 | 1,125.00 | 2.22 | mid-single digit to low double-digit royalties, per FibroGen's 6Q21 | $1.1B in option, clinical, regulatory, and commercial milestone payments across all three programs, per FibroGen's 6Q21 | ||||||||||||||||||||||||||||||
11 | 06/2021 | iTeos Therapeutics | 2013-21 IPOs | GlaxoSmithKline | Top Pharma | Co-Development, Co-Promotion, License | Phase I | 2,075.00 | 625.00 | EOS-448 anti-TIGIT monoclonal antibody to treat cancer | Link | 18817 | iTeos_GSK_0611.pdf | 50.00 | Yes | Yes | SEC Redacted | Exclusive | Cancer | Broad Focus Cancer | Monoclonals | Worldwide | EOS-448 | Immuno-Oncology | TIGIT | Inhibitor | 550.00 | 1,175.00 | 900.00 | 2,075.00 | 30.12 | 26.51 | 43.37 | 50.00 | ROW double-digit royalties up to 20%, per iTeos' 6Q21 | 50% US PS, per iTeos' 6Q21 | $900M, based on $1.45 billion in agg milestones, per iTeos' 6Q21 | $550M in agg dev/reg milestones for 3 indications | |||||||||||||||||||
12 | 06/2021 | Kyowa Hakko Kirin | Japanese Pharma | Amgen | Major Biotech, Top Pharma | Co-Development, Co-Promotion, License, Option | Phase II | 1,250.00 | 400.00 | KHK4083 anti-OX40 fully human mAb to treat atopic dermatitis ex-Japan | Link | 18710 | KyowaKirin_Amgen_060121.pdf | Yes | PR | Dermatologic | Dermatitis | Monoclonals | Human Abs | Africa, Asia, Europe, Middle East, NAFTA, South America | All African Countries, All European Countries, All Middle East Countries, All NAFTA Countries, All South American Countries, Australia, China, India, New Zealand, Other Asian, Southeast Asia | KHK4083 | Anti-Inflammatory | tumor necrosis factor receptor superfamily, member 4 (TNFRSF4) (CD134) (LY-70) (OX40) (TXGP1L) (TXGP1) (ACT35) | Inhibitor | 1,250.00 | 32.00 | 400 | Kyowa Kirin and Amgen will share global development costs, except in Japan, and U.S. commercialization costs | $850M in milestones | ||||||||||||||||||||||||||
13 | 06/2021 | MacroGenics | 2013-21 IPOs | Zai Laboratory | 2013-21 IPOs | Co-Development, Equity, License, Option | Lead Molecule, Discovery | 1,455.00 | 25.00 | Up to four CD3- or CD47-based bispecific antibodies for immuno-oncology indications | Link | 18839 | MacroGenics_Zai_0621.pdf | 30.00 | Yes | Yes | SEC Redacted | Exclusive | Cancer | Solid Tumors | Monoclonals | Bispecific | Asia | China, Japan, Other Asian | 30.00 | 800.00 | 855.00 | 600.00 | 1,455.00 | 3.78 | 54.98 | 41.24 | 50.00 | $600M for Licensed Only Products, per MacroGenics' 6Q21 | $30M in MacroGenics’ common stock at $31.30/sh, 50% premium to FMV, per MacroGenics' 6Q21 | mid single-digit to low teen royalties, per MacroGenics' 6Q21 | $800M in agg dev/reg milestones, per MacroGenics' 6Q21 | Zai has option to convert Lead Program to global 50% PS upon payment of $85M plus cost reimb, per MacroGenics' 6Q21 | ||||||||||||||||||||
14 | 06/2021 | Merck | Top Pharma | Department of Health and Human Services | Research Institution | Supply | Phase III | 1,200.00 | 1.7 million doses of molnupiravir (MK-4482) to treat COVID-19 | Link | 18818 | Merck_HHS_060921.pdf | Yes | PR | Infectious-Viral | Coronavirus | Synthetics | Small Molecule | molnupiravir, MK-4482, EIDD-2801 | Antiviral | 2019-nCoV (SARS-CoV-2) (COVID-19) | 1,200.00 | ||||||||||||||||||||||||||||||||
15 | 06/2021 | Nuvalent | 2013-21 IPOs | Deerfield Management | Equity | 50.00 | Launch of Nuvalent with $50M Series A financing | Link | 18834 | Nuvalent_Deerfield_012721.pdf | 50.00 | Yes | PR | Cancer | Synthetics | Small Molecule | 50.00 | 50.00 | 100.00 | $50M Series A financing | ||||||||||||||||||||||||||||||||||
16 | 06/2021 | Ocuphire Pharma | Processa Pharmaceuticals | Equity, License | Phase II | 228.25 | 0.20 | RX-3117 (roducitabine) for treatment of pancreatic cancer ex-Greater China & Singapore | Link | 19204 | Ocuphire_Processa_0621_Lic_Full.pdf | 0.30 | 7.50 | Yes | Yes | SEC Full | Exclusive | Cancer | Pancreatic | Synthetics | Small Molecule | Africa, Asia, Europe, Middle East, NAFTA, South America | All African Countries, All European Countries, All Middle East Countries, All NAFTA Countries, All South American Countries, Australia, India, Japan, New Zealand, Other Asian | roducitabine, RX-3117 | DNA/RNA Disruption | DNA synthesis, RNA synthesis | Inhibitor | 0.30 | 12.50 | 7.75 | 20.75 | 207.50 | 228.25 | 0.22 | 5.48 | 90.91 | 7.50 | 7.50 | 7.50 | 7.50 | 44.7K shares @ $6.71/sh | $12.5M for 1st indication | $7.75M for 2nd | |||||||||||||
17 | 06/2021 | Opko Health, EirGen Pharma | Nicoya Therapeutics | License | Phase III | 125.00 | 5.00 | Rayaldee to treat secondary hyperparathyroidism in chronic kidney disease in Greater China | Link | 18858 | Opko_Nicoya_062121.pdf | Yes | PR | Endocrinological & Metabolic | Thyroid Disease | Synthetics | Small Molecule | Asia | China | Rayaldee, Rayaldy, calcifediol, CTAP-101, JTT-762 | calcitonin receptor (CALCR) | Agonist | 5.00 | 125.00 | 4.00 | 4.00 | Tiered, double-digit royalties | $5M payment made during the first 12 months of the agreement or upon Nicoya achieving a certain predetermined development milestone | Up to $115M in development, regulatory and sales-based milestones | |||||||||||||||||||||||||||
18 | 06/2021 | PhaseBio | 2013-21 IPOs | Alfasigma USA | License | Phase III | 245.00 | 20.00 | Bentracimab to reverse antiplatelet effects of ticagrelor in Europe | Link | 18856 | PhaseBio_Alfasigma_061721.pdf | Yes | PR | Exclusive | Hematologic | Other Hematologic | Monoclonals | Fragments | Europe | Eastern Europe, European Union, Other European, Russia, United Kingdom | bentracimab, MEDI-2452, PB-2452 | Antiplatelet | 35.00 | 55.00 | 190.00 | 245.00 | 8.16 | 14.29 | 77.55 | Tiered royalties ranging from low double digits to mid-twenties | $35M in pre-revenue regulatory milestones | |||||||||||||||||||||||
19 | 06/2021 | Proteros biostructures | AstraZeneca | Top Pharma | License, Research | Discovery | 75.00 | Structure-based drug discovery to identify small molecules to treat various types of cancer | Link | 18725 | Proteros_AZ_060221.pdf | Yes | PR | Cancer | Broad Focus Cancer | Synthetics | Small Molecule | 75.00 | tiered royalties | AZ will provide research funding and Proteros is eligible for success-based research, development, and commercial milestone payments up to 62 million EUR (US$75M) | |||||||||||||||||||||||||||||||||||
20 | 06/2021 | Shenzhen Pregene Biopharma | Dr. Reddy's Laboratories | Mid Tier Pharma | License, Supply | Phase I, Orphan Indication | 162.50 | PRG1801 anti-BCMA CAR-T therapy injection to treat multiple myeloma in India | Link | 18910 | Pregene_DrReddys_051321.pdf | Yes | PR | Exclusive | Cancer | Multiple Myeloma | Cell Therapy - Stem Cells/Factors | Asia | India | PRG1801 | Immunotherapy | T lymphocyte, B-cell maturation antigen (BCMA) | Replacer | 162.50 | Double-digit royalty, up to $150 M | $5M in upfront payment and future milestone payments for first indication and up to $7.5M in milestones for subsequent indications | |||||||||||||||||||||||||||||
21 | 06/2021 | Shoreline Biosciences | Gilead, Kite Pharma | Major Biotech, 2013-21 IPOs | License, Option | 2,300.00 | Allogeneic cell therapies with focus on chimeric antigen receptor NK targets for hematologic cancers | Link | 18844 | Shoreline_Kite_061721.pdf | Yes | PR | Cancer | Leukemia, Lymphoma, Multiple Myeloma | Cell Therapy - Stem Cells/Factors | 2,300.00 | undisclosed upfront payment | Kite invested in Shoreline's April $43M series A financing | $2.3 billion in additional payments if certain development and commercial goals are met | |||||||||||||||||||||||||||||||||||||
22 | 06/2021 | Spero Therapeutics | 2013-21 IPOs | Pfizer | Top Pharma | Equity, License | Phase I | 120.00 | SPR206 to treat multi-drug resistant Gram-negative infections ex-US and ex-Asia | Link | 18956 | Spero_Pfizer_0621_Lic.pdf | 40.00 | Yes | Yes | SEC Redacted | Exclusive | Infectious-Bacterial | Other Infectious-Bacterial | Synthetics | Small Molecule | Africa, Europe, Middle East, NAFTA, South America | All African Countries, All European Countries, All Middle East Countries, All South American Countries, Canada, Mexico | SPR206 | Antibacterial | 40.00 | 120.00 | 120.00 | 33.33 | 2,362,348 shares of common at $16.93/sh (45% premium over FMV), per Spero's 6Q21 | High single digit to low double-digit royalties, per Spero's 6Q21 | $80M in agg milestones, per Spero's 6Q21 | ||||||||||||||||||||||||
23 | 06/2021 | Verona Pharmaceuticals | 2013-21 IPOs | Nuance Biotech | Equity, License | Phase III | 219.00 | 25.00 | Ensifentrine PDE3 and PDE4 dual inhibitor for respiratory indications in Greater China | Link | 18820 | Verona_Nuance_061021.pdf | Yes | PR | Exclusive | Respiratory | Asthma, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis | Synthetics | Small Molecule | Asia | China | ensifentrine, RPL 554, LS-193855 | Enzyme Inhibitor | phosphodiesterase-4 (PDE-4), phosphodiesterase-3 (PDE-3) | Inhibitor | 15.00 | 219.00 | 18.26 | Tiered double-digit royalties | $179M in clinical, regulatory, and commercial milestones | |||||||||||||||||||||||||
24 | 06/2021 | Vivoryon Therapeutics | Simcere Pharmaceutical | License, Option | Phase II, Preclinical | 565.00 | Varoglutamstat and PBD-C06 N3pE amyloid-targeting medicines for Alzheimer’s disease in Greater China | Link | 18955 | Vivoryon_Simcere_062921.pdf | Yes | PR | Central Nervous System | Alzheimer's Disease | Monoclonals, Synthetics | Humanized Abs, Small Molecule | Asia | China | varoglutamstat, PQ-912, PBD-C06 | Enzyme Inhibitor | glutaminyl-peptide cyclotransferase (QPCT) (glutaminyl cyclase) (QC), beta-amyloid (AB) | Inhibitor | 565.00 | double-digit royalties | Undisclosed upfront payment and development and sales milestones totaling $565M | ||||||||||||||||||||||||||||||
25 | 05/2021 | Agenus | 1991-2001 IPOs | Bristol-Myers Squibb | Top Pharma | Co-Promotion, Development, License, Option | Preclinical | 1,560.00 | 200.00 | AGEN1777 bispecific anti-TIGIT antibody program and related products for immuno-oncology indications | Link | 18636 | Agenus_BMS_0521.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Broad Focus Cancer | Monoclonals | Bispecific | Worldwide | AGEN-1777 | Immuno-Oncology | TIGIT | Inhibitor | 1,560.00 | 1,560.00 | 12.82 | low double-digit to mid-teen royalties, per Agenus' 6Q21 | $1.36B in agg milestones, per Agenus' 6Q21 | ||||||||||||||||||||||||
26 | 05/2021 | Calithera Biosciences | 2013-21 IPOs | Antengene | License | Preclinical | 255.00 | 3.00 | CB-708 (ATG-037) CD73 inhibitor to treat cancer | Link | 18890 | Calithera_Antengene_051721.pdf | Yes | PR | Exclusive | Cancer | Synthetics | Small Molecule | Worldwide | CB-708, ATG-037 | Enzyme Inhibitor | ecto-5'-nucleotidase (NT5E) (NT) (CD73) | Inhibitor | 255.00 | 255.00 | 1.18 | $3M, per Calithera's 6Q21 | Low double-digit royalties, per Calithera's 6Q21 | $252M in agg milestones, per Calithera's 6Q21 | |||||||||||||||||||||||||||
27 | 05/2021 | Capsigen | Biogen | Major Biotech | License, Research | Discovery, Orphan Indication | 1,307.00 | 15.00 | TRADE platform to develop AAV capsids to deliver targeted gene therapy treatments for CNS disorders | Link | 18617 | Capsigen_Biogen_051021.pdf | Yes | PR | Exclusive | Central Nervous System, Other/Miscellaneous | Genetic Disorders, Other Central Nervous System | Drug Delivery, Oligonucleotides | Gene Therapy, Other | 42.00 | 1,307.00 | 1.15 | undisclosed royalties | $1.25 billion in development and commercial payments | |||||||||||||||||||||||||||||||
28 | 05/2021 | Exscientia | Bristol-Myers Squibb | Top Pharma | License, Option | Discovery | 1,200.00 | 50.00 | AI-based platform to discover small molecule candidates for multiple therapeutic areas | Link | 18658 | Exscientia_BMS_051921.pdf | Yes | PR | Autoimmune/Inflammatory, Cancer | Bioinformatics, Synthetics | Small Molecule | 125.00 | 1,200.00 | 4.17 | 10.42 | Undisclosed tiered royalties | $125M in near to mid-term potential milestones | Clinical, regulatory and commercial payments for potential value of the deal beyond $1.2 billion | ||||||||||||||||||||||||||||||||
29 | 05/2021 | G2 Bio Companies | Temasek | Equity | Orphan Indication | 200.00 | $200M financing to launch G2 Bio Companies to develop UPenn Gene Therapy Program | Link | 18637 | G2Bio_Temasek_051821.pdf | Yes | PR | Other/Miscellaneous | Genetic Disorders | Oligonucleotides | Gene Therapy | 200.00 | 200.00 | 100.00 | UPenn and Dr. Wilson hold equity interests in the G2 Bio Companies, and will be entitled to receive licensing revenues | ||||||||||||||||||||||||||||||||||
30 | 05/2021 | Ginkgo Bioworks | Biogen | Major Biotech | License | 120.00 | 5.00 | Mammalian cell programming technology to improve AAV production platform to develop gene therapies | Link | 18655 | Ginkgo_Biogen_052121.pdf | Yes | PR | Oligonucleotides | Gene Therapy | 120.00 | 4.17 | $115M in research, development, and commercial milestones | ||||||||||||||||||||||||||||||||||||
31 | 05/2021 | Innoviva | 2003-12 IPOs | GlaxoSmithKline | Top Pharma | Equity | 392.00 | Buyback of 32% equity stake | Link | 18662 | GSK_Innoviva_052021.pdf | Yes | PR | 392.00 | ||||||||||||||||||||||||||||||||||||||||
32 | 05/2021 | Landos Biopharma | 2013-21 IPOs | LianBio | License | Phase II, Phase I | 218.00 | 18.00 | Omilancor and NX-13 to treat ulcerative colitis and Crohn’s disease in Greater China | Link | 18721 | Landos_Lian_051721.pdf | Yes | PR | Exclusive | Gastrointestinal | IBD - Crohn's Disease, IBD - Ulcerative Colitis, Other Gastrointestinal | Synthetics | Small Molecule | Asia | China, Other Asian | omilancor, BT-11, NX-13 | Anti-Inflammatory | LanC like 2 (LANCL2), NF-kappa-B essential | Agonist, Modulator | 218.00 | 8.26 | Tiered low double-digit royalties | Up to $200M in development and commercial milestones | ||||||||||||||||||||||||||
33 | 05/2021 | Milestone Pharmaceuticals | Ji Xing Pharmaceuticals | Equity, License, Supply | Phase III, Formulation | 127.50 | 15.00 | Etripamil (nasal calcium channel blocker) for cardio supraventricular tachycardia in Greater China | Link | 18651 | Milestone_JiXing_0521.pdf | 5.00 | Yes | Yes | SEC Redacted | Exclusive | Cardiovascular | Broad Focus Cardiovascular | Drug Delivery, Synthetics | Nasal, Small Molecule | Asia | China | etripamil, MSP-2017 | calcium channel | Antagonist | 5.00 | 15.50 | 35.50 | 92.00 | 127.50 | 15.69 | 12.16 | 72.16 | $92M, per Milestone's 6Q21 | $5M of pre-funded warrants, per Milestone's 6Q21 | low to high double-digit royalty, per Milestone's 6Q21 | $15.5M, per Milestone's 6Q21 | ||||||||||||||||||||
34 | 05/2021 | MiNA Therapeutics | Lilly | Top Pharma | License, Research | Discovery | 1,250.00 | 25.00 | Small activating RNA (saRNA) technology platform for up to 5 targets | Link | 18615 | MiNA_Lilly_051121.pdf | Yes | PR | Exclusive | Oligonucleotides | 1,250.00 | 2.00 | $245M in development and commercialization milestones/target | Tiered low-single to low-double digit royalties | |||||||||||||||||||||||||||||||||||
35 | 05/2021 | Mirati Therapeutics | Zai Laboratory | 2013-21 IPOs | Co-Promotion, License, Option, Supply | Phase II | 338.00 | 65.00 | Adagrasib (MTRX849 small-molecule KRASG12C inhibitor) for lung cancer in Greater China | Link | 18708 | Mirati_Zai_0521.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Colorectal, Lung | Synthetics | Small Molecule | Asia | China | adagrasib, MRTX849 | Immunomodulator | KRASG12C | Inhibitor | 93.00 | 158.00 | 180.00 | 338.00 | 19.23 | 27.51 | 53.25 | $180M, per Mirati's 6Q21 | High-teen to low twenties royalties, per Mirati's 6Q21 | $93M, per Mirati's 6Q21 | ||||||||||||||||||||
36 | 05/2021 | Nanobiotix | 2013-21 IPOs | LianBio | License | Phase III | 240.00 | NBTXR3 radioenhancer cancer treatment in Greater China | Link | 18722 | NANOBIOTIX_LianBio_051121.pdf | Yes | PR | Exclusive | Cancer | Broad Focus Cancer | Synthetics | Small Molecule | Asia | China, Other Asian | Hensify, hafnium oxide, NBTXR3, NBTX 3, PEP-503 | Radiosensitiser | 240.00 | |||||||||||||||||||||||||||||||
37 | 05/2021 | Pieris Pharmaceuticals | Roche, Genentech | Major Biotech, Top Pharma | License, Option, Research | Discovery | 1,420.00 | 20.00 | Anticalin platform to develop protein-based drugs for respiratory and ophthalmic indications | Link | 18678 | Pieris_Genentech_052521.pdf | Yes | PR | Ophthalmic, Respiratory | Broad Focus Ophthalmic, Broad Focus Respiratory | Recombinant DNA | 1,420.00 | 1.41 | Tiered royalties | $1.4 billion in milestone payments across multiple programs | ||||||||||||||||||||||||||||||||||
38 | 04/2021 | Alimera Sciences | 2003-12 IPOs | Ocumension Therapeutics | Equity, License | 109.00 | 10.00 | Iluvien for diabetic macular edema in Greater China, S Kore & ASEAN | Link | 18605 | Alimera_Ocumension_0421_Lic.pdf | 10.00 | Yes | Yes | SEC Redacted | Exclusive | Ophthalmic | Other Ophthalmic | Asia | China, Other Asian, Southeast Asia | Iluvien, Medidur FA, fluocinolone acetonide intravitreal implant, DF-277, NSC-92339 | Anti-Inflammatory | glucocorticoid receptor (GCCR) | Agonist | 10.00 | 20.00 | 89.00 | 109.00 | 18.35 | 81.65 | ||||||||||||||||||||||||
39 | 04/2021 | Bristol-Myers Squibb | Top Pharma | Agios Pharmaceuticals | 2013-21 IPOs | Equity | 344.50 | Repurchase of 7,121,658 shares of Agios common stock | Link | 18749 | Agios_BMS_0321_Eq_Full.pdf | Yes | Yes | SEC Full | 344.50 | |||||||||||||||||||||||||||||||||||||||
40 | 04/2021 | CRISPR Therapeutics | 2013-21 IPOs | Vertex | Major Biotech | Co-Development, License, Restatement | Phase II | 1,100.00 | 900.00 | CTX001 for beta thalassemia & sickle cell diseases | Link | 18570 | CRISPR_Vertex_1015_Restated_0421.pdf | 40.00 | Yes | Yes | SEC Redacted | Exclusive | Hematologic | Sickle Cell Disease, Other Hematologic | Oligonucleotides | Gene Therapy | Worldwide | CTX001 | Gene Therapy | 200.00 | 1,100.00 | 1,100.00 | 81.82 | 18.18 | 40.00 | high single-digit to mid-teen royalty if opt-out, per Crispr's 3Q31 | 40% PS to Crispr on CTX001, 50% on other Products, so long as no opt-out | ||||||||||||||||||||||
41 | 04/2021 | CureVac | 2013-21 IPOs | GlaxoSmithKline | Top Pharma | Co-Development, License, Supply | Discovery | 180.00 | 90.00 | Second-generation mRNA vaccine to address emerging COVID-19 variants | Link | 18073 | Curevac_GSK_0421_Covid.pdf | Yes | Yes | SEC Redacted | Exclusive | Infectious-Viral | Coronavirus | Vaccines | Worldwide | 180.00 | 180.00 | 50.00 | €75M ($US90M) | sub-teen to mid-teen royalties on Combination Products, per CureVac's 2020 20-F | €75M in aggregate milestones ($US90M), per CureVac's 2020 20-F | CON profit split on all but Combination Products, per CureVac's 2020 20-F | |||||||||||||||||||||||||||||
42 | 04/2021 | Lineage Cell Therapeutics | 1991-2001 IPOs | Immunomic Therapeutics | License, Research | Orphan Indication | 69.00 | 2.00 | VAC platform to develop allogeneic cell-based cancer immunotherapy vaccine candidate | Link | 18528 | Lineage_Immunomic_042021.pdf | 10.00 | Yes | PR | Exclusive | Cancer | Brain | Cell Therapy - Stem Cells/Factors, Vaccines | Worldwide | 69.00 | 2.90 | 10.00 | $67M in development and commercial milestones | ||||||||||||||||||||||||||||||
43 | 04/2021 | LogicBio Therapeutics | 2013-21 IPOs | CANbridge Life Sciences | Development, License, Option | Orphan Indication | 601.00 | 10.00 | AAV sL65 capsid to develop gene therapies for Fabry disease, Pompe disease and option to LB-001 | Link | 18552 | LogicBio_CANbridge_0421.pdf | Yes | Yes | SEC Redacted | Exclusive | Other/Miscellaneous | Genetic Disorders | Oligonucleotides | Gene Therapy | Worldwide | 601.00 | 601.00 | 1.66 | $542M in agg milestones for sL65 to treat Fabry & Pompe diseases, plus $49M in agg milestones for LB-001, per LogicBio's 6Q21 | mid- to high- single digit royalty for sL65, per LogicBio's 6Q21 | |||||||||||||||||||||||||||||
44 | 04/2021 | Mirum Pharmaceuticals | 2013-21 IPOs | CANbridge Life Sciences | License | Phase II, Orphan Indication | 120.00 | 11.00 | Maralixibat for rare liver diseases in China | Link | 18564 | Mirum_CANbridge_042921.pdf | Yes | PR | Exclusive | Liver & Gallbladder Diseases, Other/Miscellaneous | Genetic Disorders, Other Liver & Gallbladder Diseases | Synthetics | Small Molecule | Asia | China | maralixibat, LUM001, SD-5613, SHP625 | Anti-Inflammatory | solute carrier family 10 sodium-dependent bile acid transporter member 2 (SLC10A2) (ASBT) (IBAT) | Inhibitor | 120.00 | 9.17 | double-digit tiered royalties | $109M in regulatory and commercial milestones | ||||||||||||||||||||||||||
45 | 04/2021 | Obsidian Therapeutics | Vertex | Major Biotech | Equity, License, Option, Research | Discovery | 1,375.00 | 75.00 | cytoDRiVE platform to discover controllable gene editing therapies for undisclosed diseases | Link | 18538 | Obsidian_Vertex_042221.pdf | Yes | PR | Oligonucleotides | Gene Therapy | Worldwide | 1,375.00 | 5.45 | $75M in upfront payments and research milestones paid during the research term, including equity investment | $1.3 billion in research, development, regulatory, and commercial milestones across up to five programs. | ||||||||||||||||||||||||||||||||||
46 | 04/2021 | OyaGen | Tonix Pharmaceuticals | Equity, License | Preclinical | 170.00 | TNX-3500 (sangivamycin) SARS-CoV-2 inhibitor and related compounds to treat COVID-19 | Link | 18531 | Tonix_Oyagen_0421_Lic.pdf | Yes | Yes | SEC Redacted | Exclusive | Infectious-Viral | Coronavirus | Worldwide | sangivamycin, TNX-3500 | 2019-nCoV (SARS-CoV-2) (COVID-19) | Inhibitor | 170.00 | 2.75M Tonix shares issued on signing, per Tonix's 3Q21 | ||||||||||||||||||||||||||||||||
47 | 04/2021 | Pfizer | Top Pharma | Celcuity | 2013-21 IPOs | Equity, License | Phase I | 345.00 | 5.00 | Gedatolisib (PI3K & mTOR inhibitor) for breast cancer | Link | 19216 | Celcuity_Pfizer_0421_Lic.pdf | 5.00 | 05/2021 | Yes | SEC Redacted | Exclusive | Cancer | Breast | Synthetics | Small Molecule | Worldwide | gedatolisib, PF-05212384, PF-5212384, PKI-587 | Enzyme Inhibitor | mechanistic target of rapamycin (serine/threonine kinase) (mTOR) (FRAP) (FRAP1) (FRAP2) (RAFT1) (RAPT1), phosphoinositide 3-kinase (PI3K) | Inhibitor | 5.00 | 345.00 | 345.00 | 2.90 | Low to mid-teen royalties, per Celcuity's 6Q21 | $335M in agg milestones, per Celcuity's 6Q21 | ||||||||||||||||||||||
48 | 04/2021 | Senti Bio | Roche, Spark Therapeutics | Top Pharma, 2013-21 IPOs | License, Option, Research | Orphan Indication | 645.00 | Smart Sensors gene circuit technology to develop CNS, eye or liver-directed gene therapies | Link | 18511 | Senti_Spark_041321.pdf | Yes | PR | Exclusive | Other/Miscellaneous | Genetic Disorders | Oligonucleotides | Gene Therapy | 645.00 | Upfront, opt-in and milestone payments exceeding $645M | ||||||||||||||||||||||||||||||||||
49 | 03/2021 | Anima Biotech | Takeda | Top Pharma | License, Option, Research | Discovery, Orphan Indication | 1,220.00 | 120.00 | Translation Control Therapeutics platform to discover mRNA translation modulators for CNS diseases | Link | 18392 | Anima_Takeda_031821.pdf | Yes | PR | Exclusive | Central Nervous System, Other/Miscellaneous | Broad Focus Central Nervous System, Genetic Disorders | Synthetics | Small Molecule | 1,220.00 | 9.84 | $120M in upfront and preclinical research milestones | Undisclosed tiered royalties | $1.1 billion in clinical and commercial milestones for all three programs | ||||||||||||||||||||||||||||||||
50 | 03/2021 | ATAI Life Sciences, Perception Neuroscience | 2013-21 IPOs | Otsuka Pharmaceutical | Top Pharma, Japanese Pharma | License | Phase I | 121.00 | 20.00 | PCN-101 (arketamine) for depression in Japan | Link | 18777 | Perception(ATAI)_Otsuka_0321.pdf | Yes | SEC Redacted | Exclusive | Psychiatric | Depression & Mania | Synthetics | Separations | Asia | Japan | arketamine, PCN-101 | Antidepressants/Antipsychotics | NMDA receptor | Antagonist | 35.00 | 55.00 | 66.00 | 121.00 | 16.53 | 28.93 | 54.55 | $66M, per ATAI's IPO prospectus | double-digit royalties, per ATAI's IPO prospectus | $35M, per ATAI's IPO prospectus | ||||||||||||||||||||
51 | 03/2021 | Biolojic Design | Lilly | Top Pharma | Equity, License, Research | Discovery | 121.00 | AI-based multibody platform to discover antibody-based therapy to treat diabetes | Link | 18355 | Biolojic_Lilly_030821.pdf | Yes | PR | Endocrinological & Metabolic | Diabetes | Bioinformatics, Monoclonals | 121.00 | Tiered royalties in the low- to mid-single digits | $121M in development and commercialization milestones and a promissory note that may be convertible into Biolojic equity at a future date | ||||||||||||||||||||||||||||||||||||
52 | 03/2021 | BridgeBio, QED Therapeutics | 2013-21 IPOs | Helsinn | Co-Development, Co-Promotion, License | Filed | 2,000.00 | Infigratinib for cancer indications in US and all indications ex-skeletal dysplasias ex-US and China | Link | 18467 | QED_Helsinn_033121.pdf | Yes | PR | Exclusive | Cancer | Synthetics | Small Molecule | infigratinib, BGJ398 | Receptor | fibroblast growth factor (FGF) receptor (FGFR) | Inhibitor | 2,000.00 | Undisclosed tiered royalties | BridgeBio is eligible to receive more than $2 billion in upfront, regulatory and commercial milestones | |||||||||||||||||||||||||||||||
53 | 03/2021 | Cidara Therapeutics | 2013-21 IPOs | Johnson & Johnson, Janssen | Top Pharma | Co-Promotion, Development, License, Option, Research | Preclinical, Discovery | 780.00 | 27.00 | CD388 Cloudbreak antiviral conjugate to prevent and treat influenza | Link | 18484 | Cidara_Janssen_0321.pdf | Yes | Yes | SEC Redacted | Exclusive | Infectious-Viral | Influenza | Monoclonals | Fragments | Worldwide | 58.00 | 780.00 | 780.00 | 3.46 | $58M in sponsored R&D, per Cidara's 3Q21 | mid- to high- single digit royalty, per Cidara's 3Q21 | $695M in agg milestones, per Cidara's 3Q21 | |||||||||||||||||||||||||||
54 | 03/2021 | Eirion Therapeutics | Shanghai Haohai Biological Technology | Equity, License, Supply | Phase II, Preclinical | 526.00 | 8.00 | ET-01 and AI-09 for aesthetic indications; , ET-02 and ET-03 to treat hair loss in China | Link | 18334 | Eirion_Haohai_030921.pdf | Yes | PR | Exclusive | Dermatologic | Hair Disorders, Other Dermatologic | Drug Delivery, Synthetics | Small Molecule, Topical | Asia | China | 31.00 | 43.00 | 444.00 | 526.00 | 7.41 | 8.17 | 84.41 | $444M in sales milestones | $31M in Series A Preferred Stock investment | Royalty rates ranging from high single digits to the low twenties | $43M in development fees | ||||||||||||||||||||||||||
55 | 03/2021 | Genevant Sciences | Takeda | Top Pharma | License | Discovery | 600.00 | LNP technology to develop nucleic acid therapeutics for liver fibrosis | Link | 18379 | Genevant_Takeda_031521.pdf | Yes | PR | Liver & Gallbladder Diseases | Other Liver & Gallbladder Diseases | Oligonucleotides | Worldwide | 600.00 | $600M in upfront and milestone payments | |||||||||||||||||||||||||||||||||||
56 | 03/2021 | Merck | Top Pharma | BARDA | Research Institution | Supply | 268.80 | Funding to expand manufacturing capacity for SARS-CoV-2/COVID-19 vaccines and medicines | Link | 18299 | Merck_BARDA_Janssesn_030221.pdf | Yes | PR | Infectious-Viral | Coronavirus | Vaccines | 268.80 | |||||||||||||||||||||||||||||||||||||
57 | 03/2021 | Ovid Therapeutics | 2013-21 IPOs | Takeda | Top Pharma | License | Phase II, Orphan Indication | 856.00 | 196.00 | Soticlestat (TAK-935/OV935) to treat rare developmental and epileptic encephalopathies | Link | 18804 | Takeda_Ovid_030321.pdf | Yes | PR | Exclusive | Central Nervous System, Other/Miscellaneous | Epilepsy, Other Central Nervous System | Synthetics | Small Molecule | Worldwide | soticlestat, TAK-935/OV935 | Enzyme Inhibitor | cholesterol 24-hydroxylase, NMDA receptor | Inhibitor, Modulator | 856.00 | 22.90 | Tiered royalties ranging from low double-digits and up to 20% | $660M in development, regulatory and commercial milestones | ||||||||||||||||||||||||||
58 | 03/2021 | ReViral | LianBio | License | Phase II | 119.00 | 14.00 | Sisunatovir small molecule to treat RSV in China | Link | 18311 | ReViral_LianBio_030221.pdf | Yes | PR | Infectious-Viral | Respiratory Syncytial Virus/RSV | Synthetics | Small Molecule | Asia | China | sisunatovir, RV-521 | Antiviral | RSV F protein | Inhibitor | 119.00 | 11.76 | Tiered low double-digit royalties | $105M in development and commercial milestones | ||||||||||||||||||||||||||||
59 | 03/2021 | Sanofi, Bioverativ | Top Pharma | Global Blood Therapeutics | 2013-21 IPOs | License | Orphan Indication | 355.25 | 2.25 | Two early-stage small molecule research programs for sickle cell disease | Link | 18415 | GlobalBlood_Sanofi_0321_Lic.pdf | Yes | Yes | SEC Redacted | Exclusive | Hematologic | Sickle Cell Disease | Synthetics | Small Molecule | Worldwide | 355.25 | 355.25 | 0.63 | Single-digit tiered royalties per 3/16/21 PR | $353M in agg milestones per 3/16/21 PR | ||||||||||||||||||||||||||||
60 | 02/2021 | Adagene | 2013-21 IPOs | Exelixis | 1991-2001 IPOs | Co-Development, License | Discovery | 791.00 | 11.00 | SAFEbody technology for masked antibody-drug conjugates to treat solid tumors | Link | 18056 | Adagene_Exelixis_0221.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Solid Tumors | Monoclonals, Peptides | Conjugates | Worldwide | 127.50 | 127.50 | 266.00 | 525.00 | 791.00 | 1.39 | 16.12 | 66.37 | $262.5M per target, per Adagene's IPO prospectus | mid-single digit royalty, per Adagene's IPO prospectus | $27.5M in dev & $100M in reg milestones per target, per Adagene's IPO prospectus | |||||||||||||||||||||||
61 | 02/2021 | Antibe Therapeutics | Nuance Biotech | License | Phase II | 100.00 | 20.00 | Otenaproxesul for pain in Greater China region | Link | 18130 | Antibe_Nuance_020921.pdf | Yes | PR | Exclusive | Autoimmune/Inflammatory, Central Nervous System | Osteoarthritis, Pain | Synthetics | Small Molecule | Asia | China | 100.00 | 20.00 | Double-digit royalty | $80M in development and sales milestones | |||||||||||||||||||||||||||||||
62 | 02/2021 | Boston Immune Technologies and Therapeutics | BeiGene | 2013-21 IPOs | Equity, License, Option | Preclinical | 125.60 | 16.60 | TNFR2 antagonist antibodies including BITR2101 for cancer in Asia ex-Japan | Link | 18239 | BITT_BeiGene_021721.pdf | 4.00 | Yes | PR | Exclusive | Cancer | Monoclonals | Asia | Australia, China, India, New Zealand, Other Asian, Southeast Asia | BITR2101 | Immuno-Oncology | tumor necrosis factor receptor 2 (TNFR2) | Antagonist | 4.00 | 125.60 | 16.40 | $16.6M inclusive of BeiGene's exercise of the option to license following initial proof-of-concept studies | $4 million in BITT’s Series A preferred stock financing | Up to $105M in development, regulatory, and sales milestones | ||||||||||||||||||||||||||
63 | 02/2021 | Caribou Biosciences | 2013-21 IPOs | AbbVie | Top Pharma | Equity, License, Option, Research | Discovery | 740.00 | chRDNA genome editing and cell therapy technologies for allogeneic CAR-T cell therapies | Link | 18157 | Caribou_AbbVie_0221.pdf | 10.00 | Yes | Yes | SEC Redacted | Exclusive | Cancer | Broad Focus Cancer | Cell Therapy - Stem Cells/Factors, Oligonucleotides | Gene Therapy | Worldwide | 740.00 | |||||||||||||||||||||||||||||||
64 | 02/2021 | Cellectis | 2013-21 IPOs | Cytovia Therapeutics | Equity, License, Research | Discovery | 775.00 | Up to five TALEN gene-edited iPSC NK and CAR-NK cell therapeutics to treat cancer | Link | 18214 | Cellectis_Cytovia_021621.pdf | 15.00 | Yes | PR | Cancer | Broad Focus Cancer | Cell Therapy - Stem Cells/Factors | Worldwide | 15.00 | 775.00 | 1.94 | $15M in Cytovia stock or an upfront cash payment of $15M if certain conditions are not met by 12/31/21 | single-digit royalty payments | $760M in development, regulatory, and sales milestones | ||||||||||||||||||||||||||||||||
65 | 02/2021 | Cend Therapeutics | Qilu Pharmaceutical | License | Phase I | 235.00 | 10.00 | CEND-1 for pancreatic cancer and other solid tumors in Greater China | Link | 18243 | Cend_Qilu_021621.pdf | Yes | PR | Exclusive | Cancer | Pancreatic, Solid Tumors | Peptides | Asia | China | 235.00 | 4.26 | Tiered double digit royalties | $225M in undisclosed milestones | ||||||||||||||||||||||||||||||||
66 | 02/2021 | Dana-Farber | Research Institution | Deerfield Management | Research | 130.00 | $130M over 10 years to fund translational research at Dana-Farber | Link | 18119 | DanaFarber_Deerfield_020821.pdf | Yes | PR | 130.00 | 130.00 | Up to $130M over 10 years | |||||||||||||||||||||||||||||||||||||||
67 | 02/2021 | Ensoma | Takeda | Top Pharma | Equity, License, Research | Discovery, Orphan Indication | 1,360.00 | 100.00 | Engenious vector technology platform for up to five rare genetic disease indications | Link | 18172 | Ensoma_Takeda_021121.pdf | 10.00 | Yes | PR | Exclusive | Other/Miscellaneous | Genetic Disorders | Oligonucleotides | Gene Therapy | Worldwide | 10.00 | 1,360.00 | 8.09 | $100 million in upfront and preclinical research payments | Equity investment of $10M in Ensoma’s Series A Preferred Stock | Up to low double-digit royalties | Up to $1.25 billion including development and commercialization milestone payments for all five programs | |||||||||||||||||||||||||||||
68 | 02/2021 | Gritstone Oncology | 2013-21 IPOs | Gilead | Major Biotech | Equity, License, Option, Research | 785.00 | 30.00 | Prime-boost vaccine platform to develop HIV-specific therapeutic vaccine | Link | 18051 | Gritstone_Gilead_020121.pdf | 30.00 | Yes | PR | Exclusive | Infectious-Viral | Human Immunodeficiency Virus/HIV | Vaccines | 30.00 | 785.00 | 7.64 | $725M in option, regulatory and commercial milestone payments | Mid single-digit to low double-digit tiered royalties | |||||||||||||||||||||||||||||||
69 | 02/2021 | Junshi Biosciences | Coherus Biosciences | 2013-21 IPOs | Co-Development, Equity, License, Option | Phase III, Preclinical | 1,110.00 | 150.00 | Toripalimab anti-PD-1 antibody in the US and Canada, option to JS006 and JS018-1 | Link | 18057 | Coherus_Junshi_0221_Full.pdf | 20.00 | Yes | Yes | SEC Full | Exclusive | Cancer | Broad Focus Cancer | Monoclonals | Humanized Abs | NAFTA | Canada, US | toripalimab, JS001, JS 001, TAB-001, SO-001 | Immuno-Oncology | programmed cell death 1 (PD-1) (PDCD1) (CD279) | Antagonist | 0.31 | 90.00 | 240.00 | 480.00 | 630.00 | 1,110.00 | 13.51 | 8.11 | 56.76 | 20.00 | 20.00 | 20.00 | 20.00 | 15.00 | $290M for PD-1 & $170M for each Option Product | 25% of global dev costs, up to $25M/yr cap | 20% for PD-1 and 18% for each Option Product | $90M for PD-1 indications | $35M option exercise plus $85M for each Option Product | Junshi purchased $50M of Coherus shares at FMV of $20.06/sh at signing | ||||||||||||
70 | 02/2021 | Molecular Templates | Bristol-Myers Squibb | Top Pharma | License, Option, Research | Discovery | 1,394.50 | 70.00 | Engineered toxin body platform to discover targeted therapeutics for cancer | Link | 18171 | MolTemplates_BMS_0221.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Monoclonals | Conjugates | Worldwide | 874.50 | 944.50 | 450.00 | 1,394.50 | 5.02 | 62.71 | 32.27 | $450M, per Mol Templates' 2020 10-K | mid-single digit to mid-teen royalties, per Mol Templates' 2020 10-K | $874.5M per Mol Templates' 2020 10-K | MTEM pays R&D costs thru designation of dev candidate for Initial Target | ||||||||||||||||||||||||||
71 | 02/2021 | Pacific Biosciences of California | 2003-12 IPOs | SoftBank | Loan | 900.00 | $900M investment through convertible senior notes | Link | 18155 | PacificBio_Softbank_0221_Loan_Full.pdf | Yes | Yes | SEC Full | Genomics | Gene Sequencing | 900.00 | 900.00 | 900.00 | 1.5% convertible notes, due 2028 | |||||||||||||||||||||||||||||||||||
72 | 02/2021 | Provention Bio | Hangzhou Zhongmei Huadong Pharmaceutical | License | Phase II, Orphan Indication | 189.50 | 6.00 | PRV-3279 DART molecule targeting B cell surface proteins CD32B and CD79B in Greater China | Link | 18240 | ProventionBio_Huadong_021721.pdf | Yes | PR | Autoimmune/Inflammatory | Systemic Lupus Erythematosus | Monoclonals | Bispecific | Asia | China | MGD010, PRV-3279, CD32BxCD79B | Antibody | CD79b molecule immunoglobulin-associated beta (CD79B) (B29), Fc gamma receptor IIb (FCGR2B) (CD32B) | Modulator | 11.50 | 189.50 | 3.17 | Up to $11.5 million in research, development and manufacturing funding | Low-to-mid double digit royalties | Up to $172M in development, regulatory and commercial milestones | |||||||||||||||||||||||||||
73 | 02/2021 | Ribon Therapeutics | Ono Pharmaceutical | License | Phase I | 148.30 | 16.30 | RBN-2397 PARP7 inhibitor for cancer In Japan, South Korea, Taiwan and ASEAN countries | Link | 18083 | Ribon_Ono_020221.pdf | Yes | PR | Exclusive | Cancer | Synthetics | Small Molecule | Asia | Japan, Other Asian, Southeast Asia | RBN-2397 | Enzyme Inhibitor | poly (ADP-ribose) polymerase (PARP-7) | Inhibitor | 148.30 | 10.99 | Tiered royalties ranging from the high single digits to low teens | $132M in regulatory and commercial milestones | ||||||||||||||||||||||||||||
74 | 02/2021 | Rigel Pharmaceuticals | 1991-2001 IPOs | Lilly | Top Pharma | Co-Development, Co-Promotion, License, Option, Research | Phase I, Preclinical | 960.00 | 125.00 | R552 (RIPK1 inhibitors) for autoimmune, inflammatory & CNS diseases | Link | 18238 | Rigel_Lilly_0221.pdf | Yes | Yes | SEC Redacted | Exclusive | Autoimmune/Inflammatory, Central Nervous System | Broad Focus Autoimmune/Inflammatory, Broad Focus Central Nervous System | Synthetics | Small Molecule | Worldwide | R552 | Enzyme Inhibitor | receptor (TNFRSF)-interacting serine-threonine kinase 1 (RIPK1) | Inhibitor | 330.00 | 255.00 | 710.00 | 250.00 | 960.00 | 13.02 | 34.38 | 26.04 | $100M for each auto/inflam product, and $150M for each CNS product, per Rigel's 3Q21 | mid-single digit to high-teens royalty for R552, and low double-digit for CNS, per Rigel's 3Q21 | $330M for auto/inflam products, per Rigel's 3Q21 | $255M for CNS products, per Rigel's 3Q21 | |||||||||||||||||||
75 | 02/2021 | Scynexis | 2013-21 IPOs | Jiangsu Hansoh Pharmaceutical | License | Phase III | 120.00 | 10.00 | Ibrexafungerp broad-spectrum triterpenoid antifungal in Greater China | Link | 18236 | Scynexis_Hansoh_0221.pdf | Yes | Yes | SEC Redacted | Exclusive | Infectious-Miscellaneous | Fungal | Synthetics | Small Molecule | Asia | China | ibrexafungerp | Antifungal | beta-1,3-D glucan synthetase | Inhibitor | 120.00 | 120.00 | 8.33 | low double digit royalty, per Scynexis' 3Q21 | $110M in agg milestones, per Scynexis' 3Q21 | ||||||||||||||||||||||||
76 | 02/2021 | Vir Biotechnology | 2013-21 IPOs | GlaxoSmithKline | Top Pharma | Co-Development, Equity, License, Option, Research | Phase I, Discovery | 845.00 | 225.00 | VIR-2482 for Influenza A & functional genomics to treat respiratory viruses | Link | 18596 | Vir_GSK_0221.pdf | 120.00 | 50.00 | Yes | Yes | SEC Redacted | Exclusive | Infectious-Miscellaneous, Infectious-Viral | Coronavirus, Influenza, Respiratory Syncytial Virus/RSV, Other Infectious-Miscellaneous, Other Infectious-Viral | Genomics, Screening | Gene Expression | Worldwide | VIR-2482 | Antiviral | undisclosed | 120.00 | 500.00 | 845.00 | 845.00 | 40.83 | 59.17 | 50.00 | 50/50 dev cost sharing for all programs, except Vir pays for VIR-2482 thru Ph II | $300M on option exercise, plus $200M reg milestones for VIR-2482 | |||||||||||||||||||
77 | 01/2021 | AADi | EOC Pharma | License | Orphan Indication | 271.00 | ABI-009 (FYARRO) for cancer in Greater China | Link | 18669 | Aadi_EOC_011121.pdf | Yes | PR | Exclusive | Cancer | Solid Tumors, Other Cancer | Synthetics | Small Molecule | Asia | China | Fyarro, Tarzifyx, nab-sirolimus, ABI-009, nab-rapamycin | Immunosuppresant | mechanistic target of rapamycin (serine/threonine kinase) (mTOR) (FRAP) (FRAP1) (FRAP2) (RAFT1) (RAPT1), T lymphocyte | Inhibitor | 271.00 | Tiered royalties | upfront payment, regulatory and sales milestone payments totaling up to $271M | |||||||||||||||||||||||||||||
78 | 01/2021 | Alteogen | Intas Pharmaceuticals | License, Supply | 115.00 | 6.00 | Development of two products combined with ALT-B4 Hybrozyme-enabled technology | Link | 17886 | Alteogen_Intas_010721.pdf | Yes | PR | Recombinant DNA | 115.00 | 5.22 | Tiered royalty ranging from mid-single digit to low double digit | $109M in development, regulatory and sales milestones | ||||||||||||||||||||||||||||||||||||||
79 | 01/2021 | Argenx | 2013-21 IPOs | Zai Laboratory | 2013-21 IPOs | Co-Development, Equity, License, Supply | Phase II | 175.00 | Efgartigimod antibody fragment for myasthenia gravis in Greater China | Link | 17894 | Argenx_Zai_0121_Lic.pdf | Yes | Yes | SEC Redacted | Exclusive | Autoimmune/Inflammatory | Broad Focus Autoimmune/Inflammatory, Other Autoimmune/Inflammatory | Monoclonals | Fragments | Asia | China | efgartigimod, ARGX-113 | Fc fragment of IgG, receptor, transporter, alpha (FCGRT) (FCRN) | Antagonist | 75.00 | 75.00 | 25.00 | 175.00 | 175.00 | 42.86 | 14.29 | 568.2K Zai shares @ $132/sh, per argenx' 2020 Form 20-F | $75M in dev cost reimb, per argenx' 2020 Form 20-F | Mid-teen to low twenties royalties, per argenx' 2020 Form 20-F | $25M on US approval, per argenx' 2020 Form 20-F | |||||||||||||||||||||
80 | 01/2021 | Artiva Biotherapeutics | Merck | Top Pharma | License, Option, Research | Discovery | 1,288.00 | 30.00 | Chimeric antigen receptor-NK cell therapies targeting solid tumor-associated antigens | Link | 18027 | Artiva_Merck_0121.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Solid Tumors | Cell Therapy - Stem Cells/Factors | Worldwide | 28.00 | 0.00 | 265.00 | 700.00 | 1,288.00 | 2.33 | 0.00 | 54.35 | $350M per program, per Artiva's IPO prospectus | $14M per program, per Artiva's IPO prospectus | high single-digit to low teen royalties, per Artiva's IPO prospectus | $265M for second program | 588 | |||||||||||||||||||||||||
81 | 01/2021 | Asahi Kasei | Japanese Pharma | Lilly | Top Pharma | License | Phase I | 410.00 | 20.00 | AK1780 oral P2X7 receptor antagonist for chronic pain ex-Japan and China | Link | 18023 | AsahiKasei_Lilly_012821.pdf | Yes | PR | Exclusive | Central Nervous System | Pain | Synthetics | Small Molecule | Africa, Asia, Europe, Middle East, NAFTA, South America | All African Countries, All European Countries, All Middle East Countries, All NAFTA Countries, All South American Countries, Australia, India, New Zealand, Other Asian, Southeast Asia | 210.00 | 230.00 | 180.00 | 410.00 | 4.88 | 51.22 | 43.90 | tiered royalties ranging from the mid-single to low-double digits. | ||||||||||||||||||||||||
82 | 01/2021 | BeiGene | 2013-21 IPOs | Novartis | Top Pharma | Co-Development, Co-Promotion, License, Option | Phase III | 2,200.00 | 650.00 | Tislelizumab anti-PD-1 monoclonal antibody to treat cancer in NAFTA, Europe and Japan | Link | 17953 | BeiGene_Novartis_0121.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Broad Focus Cancer | Monoclonals | Humanized Abs | Asia, Europe, NAFTA | All NAFTA Countries, Eastern Europe, European Union, Japan, Russia, Scandinavia, United Kingdom | tislelizumab, BGB-A317 | Immuno-Oncology | programmed cell death 1 (PD-1) (PDCD1) (CD279) | Inhibitor | 1,300.00 | 1,950.00 | 250.00 | 2,200.00 | 29.55 | 59.09 | 11.36 | $250M, per BeiGene's 3Q21 | $1.3B, per BeiGene's 3Q21 | |||||||||||||||||||
83 | 01/2021 | BioNTech | 2013-21 IPOs | Pfizer | Top Pharma | Co-Development, Distribution, Equity, License, Restatement | Approved | 748.00 | 72.00 | Comiranty BNT162 vaccine for COVID-19 ex-China | Link | 18569 | BioNTech_Pfizer_0320_Restated_0121.pdf | 113.00 | 50.00 | Yes | SEC Redacted | Exclusive | Infectious-Viral | Coronavirus | Oligonucleotides, Vaccines | RNAi | Africa, Asia, Europe, Middle East, NAFTA, South America | Comirnaty, Pfizer-BioNTech Covid-19 Vaccine, tozinameran, BNT162, PF-07302048, BNT162B2 | Vaccine | mRNA | 2019-nCoV (SARS-CoV-2) (COVID-19) | 113.00 | 748.00 | 748.00 | 24.73 | 50.00 | $72M in 3/20 | $113M eq in 4/20 | $563M in agg milestones, per BioNTech's 2020 20-F | |||||||||||||||||||||
84 | 01/2021 | Blacksmith Medicines | Lilly | Top Pharma | Equity, License, Research | Discovery | 300.00 | Small molecule inhibitors against up to 5 human metalloenzyme targets | Link | 17893 | Blacksmith_Lilly_010821.pdf | Yes | PR | Synthetics | Small Molecule | 300.00 | Undisclosed upfront payment | Investment from Lilly in exchange for a convertible note | Up to $60M per target in research, development and commercial milestones, total potential deal size valued at $300M. | |||||||||||||||||||||||||||||||||||||
85 | 01/2021 | Dynavax Technologies | 2003-12 IPOs | Coalition for Epidemic Preparedness Innovations | Loan | 99.00 | CpG 1018 (TLR9 agonist) adjuvant manufacturing for use in COVID-19 vaccines | Link | 18053 | Dynavax_CEPI_0121_Loan.pdf | 05/2021 | Yes | Yes | SEC Redacted | Infectious-Viral | Coronavirus | Adjuvant | CpG 1018, ISS-1018, ISS 1018 CpG ODN, CpG ODN | Immunostimulant | toll-like receptor 9 (TLR9) | 99.00 | 99.00 | 99.00 | |||||||||||||||||||||||||||||||
86 | 01/2021 | EVOQ Therapeutics | Amgen | Major Biotech, Top Pharma | License, Research | Discovery | 240.00 | Drug discovery for autoimmune disorders | Link | 17930 | EVOQ_Amgen_011321.pdf | Yes | PR | Autoimmune/Inflammatory | 240.00 | Upfront and milestone payments potentially totaling more than $240M | ||||||||||||||||||||||||||||||||||||||
87 | 01/2021 | First Wave Bio | AzurRx BioPharma | 2013-21 IPOs | Equity, License | Formulation | 87.30 | 10.25 | Oral and enema formulations of niclosamide to treat ICI-AC and COVID-19 GI infections | Link | 17868 | FirstWave_AzurRx_010421.pdf | Yes | PR | Exclusive | Gastrointestinal | Drug Delivery, Synthetics | Oral, Other, Small Molecule | Worldwide | niclosamide, ANA-001, BAY 2353, NSC-178296, WR 46234, DWRX2003 | Antiviral | signal transducer and activator of transcription 3 (STAT3) | Inhibitor | 3.00 | 87.30 | 15.18 | $10.25M in cash payable $9M at closing and $1.25M by June 30, 2021 | $3M Convertible Junior Preferred Stock | $74M in development and commercial milestones | mid single-digit royalties | |||||||||||||||||||||||||||
88 | 01/2021 | Genevant Sciences | Gritstone Oncology | 2013-21 IPOs | License | 192.00 | LNP technology to develop and commercialize self-amplifying RNA vaccines against SARS-CoV-2 | Link | 17989 | Genevant_Gritstone_012021.pdf | Yes | PR | Infectious-Viral | Coronavirus | Vaccines | 192.00 | Royalties ranging from the mid-single to the mid-double digits | $192M in upfront and milestone payments per product | |||||||||||||||||||||||||||||||||||||
89 | 01/2021 | La Jolla Pharmaceutical, TetraPhase | 2013-21 IPOs, 1991-2001 IPOs | Paion | License | Approved | 132.00 | 22.50 | Giapreza (angiotensin II) for hypotension and Xerava (eravacycline) for infections in Europe | Link | 18465 | Tetraphase(LaJolla)_Paion_0121_Lic.pdf | Yes | SEC Redacted | Exclusive | Cardiovascular, Infectious-Bacterial | Other Cardiovascular, Other Infectious-Bacterial | Synthetics | Europe | All European Countries | Giapreza, angiotensin II acetate, LJPC501 | Receptor | angiotensin II type 1 receptor (AGTR1) | Agonist | 22.50 | 109.50 | 132.00 | 17.05 | 82.95 | $24.5M for Xerava and $85M for Giapreza | double-digit royalties, per La Jolla's 2020 10-K | ||||||||||||||||||||||||
90 | 01/2021 | Merus BV | 2013-21 IPOs | Lilly, Loxo Oncology | Top Pharma, 2013-21 IPOs | Equity, License, Research | Discovery | 600.00 | 40.00 | Biclonics platform for up to three CD3-engaging T-cell re-directing bispecific antibody therapies | Link | 17972 | Merus_Lilly_0121.pdf | 20.00 | Yes | Yes | SEC Redacted | Exclusive | Cancer | Monoclonals | Bispecific | Worldwide | 20.00 | 290.00 | 350.00 | 250.00 | 600.00 | 10.00 | 48.33 | 41.67 | $250M in sales milestones per program, per Merus' 2020 10-K | 707K shares @ $28.295/sh, per Merus' 2020 10-K | mid-single to low-double digit royalty, per Merus' 2020 10-K | $290M for each program, per Merus' 2020 10-K | |||||||||||||||||||||||
91 | 01/2021 | MiNA Therapeutics | Servier | Mid Tier Pharma | License, Research | Discovery | 267.00 | Small activating RNA therapies to treat neurological disorders | Link | 17985 | MinA_Servier_012121.pdf | Yes | PR | Central Nervous System | Oligonucleotides | RNAi | 267.00 | €220 M (US$267M) in upfront, development and commercial milestonesfor first target | ||||||||||||||||||||||||||||||||||||
92 | 01/2021 | Nevakar | Laboratoires Thea | Distribution, License | Phase III | 135.00 | NVK-002 (atropine) to treat progression of myopia in children in Europe | Link | 18020 | Nevakar_Thea_012821.pdf | Yes | PR | Exclusive | Ophthalmic | Other Ophthalmic | Synthetics | Small Molecule | Africa, Europe | All European Countries, Other African | 135.00 | ||||||||||||||||||||||||||||||||||
93 | 01/2021 | Paratek Pharmaceuticals | R-Bridge Healthcare | Loan | 60.00 | Loan to be repaid using royalties from Zai collaboration to pay off Hercules Capital secured debt | Link | 17878 | Paratek_RBridge_010421.pdf | Yes | PR | 60.00 | 60.00 | |||||||||||||||||||||||||||||||||||||||||
94 | 01/2021 | TRIGR Therapeutics | Elpiscience BioPharma | License | Phase I | 117.00 | 7.00 | TR009 dual angiogenic bispecific antibody targeting DLL4/VEGF for oncology indications in China | Link | 17987 | TRIGR_Elpiscience_012021.pdf | Yes | PR | Exclusive | Cancer | Broad Focus Cancer | Monoclonals | Asia | China | 117.00 | 5.98 | $110M in development and commercial milestones | ||||||||||||||||||||||||||||||||
95 | 01/2021 | Turning Point Therapeutics | 2013-21 IPOs | Zai Laboratory | 2013-21 IPOs | License, Supply | Phase I | 361.00 | 25.00 | TPX-0022 )MET/SRC/CSF1R Inhibitor) for solid tumors in Greater China | Link | 18408 | TurningPoint_Zai_0121_Lic.pdf | 03/2021 | Yes | Yes | SEC Redacted | Exclusive | Cancer | Solid Tumors | Synthetics | Small Molecule | Asia | China | 121.00 | 146.00 | 215.00 | 361.00 | 6.93 | 33.52 | 59.56 | $215M, per Turning Point's 2020 10-K | mid-teen to low twenties royalties, per Turning Point's 2020 10-K | $121M, per Turning Point's 2020 10-K | ||||||||||||||||||||||
96 | 12/2020 | Aligos Therapeutics | 2013-21 IPOs | Merck | Top Pharma | License, Research | Discovery | 458.00 | Oligonucleotides directed against NASH target, second target in cardiometabolic/fibrosis | Link | 17768 | Aligos_Merck_120720.pdf | Yes | PR | Exclusive | Cardiovascular, Liver & Gallbladder Diseases | Fatty Liver | Oligonucleotides | 458.00 | tiered royalties | $458M in development and commercialization milestones | ||||||||||||||||||||||||||||||||||
97 | 12/2020 | Allecra Therapeutics | Yangtze River Pharmaceutical, Shanghai Haini Pharmaceutical | License | Phase III | 78.00 | Cefepime/enmetazobactam antibiotic in Greater China | Link | 17812 | Allecra_ShanghaiHaini_122120.pdf | Yes | PR | Exclusive | Infectious-Bacterial | Pneumonia, Urinary Tract Infections | Synthetics | Small Molecule | Asia | China | 78.00 | ||||||||||||||||||||||||||||||||||
98 | 12/2020 | Allogene Therapeutics | 2013-21 IPOs | Overland Pharmaceuticals | Equity, Joint Venture, License | Lead Molecule | 80.00 | 40.00 | CAR-T cell candidates to BCMA, CD70, FLT3, and DLL3 targets in China, S Korea & Singapore | Link | 18302 | Allogene_Overland_1220_Lic.pdf | 49.00 | Yes | SEC Redacted | Exclusive | Cancer | Broad Focus Cancer | Cell Therapy - Stem Cells/Factors | Asia | China, Other Asian | 40.00 | 80.00 | 80.00 | 50.00 | 50.00 | 49.00 | $40M upfront from JV, per Allogene's 2020 10-K | Overland purchase 51% of JV for $117M, per Allogene's 2020 10-K | low to mid-single digit royalties, per Allogene's 2020 10-K | $40M in reg milestones from JV, per Allogene's 2020 10-K | 49% of JV owned by Allogene, per Allogene's 2020 10-K | ||||||||||||||||||||||||||
99 | 12/2020 | Atara Biotherapeutics | 2013-21 IPOs | Bayer | Top Pharma | Co-Development, License | Phase I, Preclinical | 675.00 | 60.00 | ATA3271 and ATA2271 Mesothelin-directed CAR T-cell therapies to treat solid tumors | Link | 17726 | Atara_Bayer_1220.pdf | Yes | Yes | SEC Redacted | Exclusive | Cancer | Solid Tumors | Cell Therapy - Stem Cells/Factors | Worldwide | 5.00 | 675.00 | 675.00 | 8.89 | up to low double digit royalties, per Atara's 2020 10-K | $610M in agg milestones, per Atara's 2020 10-K | ||||||||||||||||||||||||||||
100 | 12/2020 | Chordia Therapeutics | Ono Pharmaceutical | License | Preclinical, Orphan Indication | 482.00 | 7.00 | CTX-177 MALT1 inhibitor and related compounds | Link | 19128 | Chordia_Ono_121520.pdf | Yes | PR | Exclusive | Cancer | Lymphoma | Synthetics | Small Molecule | Worldwide | CTX-177 | mucosa associated lymphoid tissue lymphoma translocation gene 1 (MALT1) | Inhibitor | 482.00 | 1.45 | JPY0.8 billion (US$7M) | High-single digits to low double-digit tiered royalties | JPY2.5 billion (US$23M) upon Phase I initiation | JPY49.6 billion (US$452M) in additional development and commercial milestones |