10 November 2026 | Tuesday | Analysis
Bars count qualifying disclosed events per institution; the label beside each bar gives the largest disclosed figure that decides its rank.
Every November, the same ritual plays out in a European convention hall. University technology-transfer offices arrive with slides counting patents filed, invention disclosures logged and startups formed. This year BIO-Europe runs from 9 to 11 November at Koelnmesse in Cologne, with digital partnering following on 17 and 18 November, and the Asia-Pacific delegations are bigger than ever.
Those slides measure activity, not conversion. A patent that never leaves the shelf is a cost centre. The question a licensing executive actually asks across the table is simpler: when this institution's science leaves campus, does anyone pay for it, and how much?
The question matters more now because Asia-Pacific has become the place where pharma shops. Chinese drugmakers alone signed 157 out-licensing deals worth US$135.7 billion in 2025, up from 94 deals worth US$51.9 billion a year earlier, according to regulator data reported by the South China Morning Post. GlobalData counted US$7.86 billion of Korean innovator licensing value in the first seven months of 2025. Almost all of those headlines name companies. The universities and institutes whose science sits underneath them are usually invisible.
This list tries to make them visible. It counts disclosed licences of drug assets and disclosed spinout financings, not patent families, and it says plainly where an institution's silence kept it out.
Inclusion. An institution qualifies if it is traceable as the IP origin of a drug asset (small molecule, biologic, oligonucleotide, vaccine or cell therapy) licensed between 1 January 2024 and 10 November 2026, either directly to a company or onward from its own spinout to a pharma partner; or as the origin of a spinout that disclosed a financing round or exit in the same window.
The ten
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Tech-transfer office |
UniQuest, the university's wholly owned commercialisation company, with its small-molecule group QEDDI (Queensland Emory Drug Discovery Initiative) |
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Licensed assets and licensees |
QED-203, a cancer candidate from Professor Greg Monteith's research developed at QEDDI: exclusive licence to the Ellison Medical Institute, Los Angeles (June 2026). Molecular Clamp vaccine platform: licensed earlier to Vicebio |
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Spinouts and rounds |
Vicebio Series B (September 2024), led by TCGX with UniQuest participating. Sanofi agreed to acquire Vicebio in July 2025 for US$1.15 billion upfront plus up to US$450 million in milestones |
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The model that works |
Licence plus equity. UQ holds Vicebio shares through both direct investment and the licence itself |
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Note |
The original Vicebio licence predates the window; the 2024 round, the 2025 exit and the 2026 QED-203 licence all fall inside it |
Queensland sits at the top because it shows the full arc that every tech-transfer office pitches and few complete. The Molecular Clamp, invented by Keith Chappell, Daniel Watterson and Paul Young, stabilises viral surface proteins in their prefusion shape. UniQuest licensed it to Vicebio, a company Medicxi built around the platform, and kept equity. When Sanofi agreed to buy Vicebio for its bivalent RSV and hMPV vaccine VXB-241, then in exploratory Phase 1, the university described it as the largest deal ever involving a company commercialising Australian university IP.
What keeps Queensland from being a one-deal story is what happened next. In June 2026 UniQuest granted an exclusive licence for QED-203 to the Ellison Medical Institute, and the asset came out of QEDDI, the in-house medicinal chemistry group that UQ and the Queensland government seeded so that academic hits would reach a licensable candidate stage before anyone asked a pharma company to pay. That is the lesson for partnering teams in Cologne: Queensland does not sell disclosures; it sells molecules with a development package attached.
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Tech-transfer office |
KAIST Technology Value Creation office, working through the faculty-startup route |
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Licensed assets and licensees |
SVG105, an antisense oligonucleotide against MTOR for drug-resistant focal cortical dysplasia epilepsy: exclusive global option to licence granted by KAIST faculty spinout Sovargen to Angelini Pharma (September 2025), excluding Korea, mainland China, Hong Kong, Macau and Taiwan. Undisclosed upfront; milestones up to about US$550 million plus tiered royalties |
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Spinouts and rounds |
Sovargen, founded in May 2018 on Professor Lee Jeong-ho's research. No new financing round with disclosed terms found inside the window |
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The model that works |
Physician-scientist founder paired with an industry drug developer as chief executive |
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Note |
KAIST valued the deal at KRW 750 billion. The asset is preclinical and the structure is an option, so the headline is contingent |
KAIST qualifies on a single deal, but it is the cleanest example in the region of basic science turning into a priced asset. Lee Jeong-ho's laboratory showed, in papers published in Nature in 2015 and Nature Medicine in 2018, that some intractable epilepsies are driven by acquired mutations in brain stem cells rather than inherited ones. Sovargen then built an antisense programme that hits the mutated MTOR pathway directly.
Korean reporting credits the turn to commercial traction to the arrival of Park Cheol-won, a former LG drug developer with global licensing experience, as co-chief executive in 2023. The Korean-language coverage also adds a timeline the English press releases omit: Sovargen is targeting global clinical entry for SVG105 in 2027. For a licensee, that is the real question behind a US$550 million headline.
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Tech-transfer office |
KIST technology-in-kind investment route, under which the institute takes equity in a company in exchange for its technology |
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Licensed assets and licensees |
CV-01, an oral small molecule acting on the Keap1 and Nrf2 pathway: exclusive option agreement between KIST-founded Cureverse and Angelini Pharma (October 2024) for global rights outside Korea, mainland China, Hong Kong, Macau and Taiwan |
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Spinouts and rounds |
Cureverse, founded in 2021 on KIST technology. No disclosed-terms round found inside the window |
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The model that works |
Institute research, equity-backed company, then a partner deal at Phase 1 |
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Note |
Korea's science ministry put the deal at US$370 million including milestones; BioWorld reported US$360 million. Both figures are shown |
KIST researchers led by Park Ki-duk had worked on CV-01 since 2014. The compound entered Phase 1 in Korea in September 2024 and was optioned to Angelini a month later, with Angelini taking the lead on development. Korean trade reporting since then says the Italian company is running a European Phase 1b in Alzheimer's disease, while Cureverse continues its domestic Phase 1 at Seoul National University Hospital.
The pairing of entries two and three is the most interesting pattern on this list. Angelini, a privately owned mid-size European company building a brain health franchise, bought into two Korean institutional assets in eleven months, both in neurology, both before proof of concept. That is a buyer profile academic offices in Asia should be studying: not big pharma, but focused specialists willing to take early CNS risk in exchange for ex-Asia rights.
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Tech-transfer office |
Office of Technology Transfer (OTT) |
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Licensed assets and licensees |
Two agreements with PharmNoah Intelligence (Suzhou) Biotech, reported in September 2025 at more than RMB 237 million in total: an exclusive patent licence for a series of small-molecule anti-neuroblastoma candidates from Professor Bai Fang's team, on upfront plus milestone terms, and exclusive commercialisation rights to the team's AI drug discovery platform |
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Spinouts and rounds |
Faculty and graduate companies licensing university patents, including Zhenxu (Shanghai) Biotechnology, which holds an exclusive global patent portfolio licence reported at more than RMB 170 million (date not disclosed, so not counted) |
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The model that works |
Exclusive licences priced into faculty-founded companies, with the terms published |
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Note |
The OTT says about 70% of its PCT and foreign patents have been licensed, with cumulative contract value above RMB 7 billion |
ShanghaiTech is the only mainland Chinese institution on this list, and the reason is disclosure rather than science. China's companies signed 157 out-licensing deals worth US$135.7 billion in 2025, according to regulator figures reported by the South China Morning Post, but the academic origin of those assets is rarely traceable in English or Chinese filings. ShanghaiTech is an exception because it publishes deal values for its own transfers.
Its track record also predates the window. An anti-schizophrenia candidate, SPH9788, was licensed to Shanghai Pharmaceuticals by ShanghaiTech and the Chinese Academy of Sciences' Center for Excellence in Molecular Cell Science around the end of 2021. A Ministry of Education case listing puts the contract at RMB 100 million, with RMB 5 million upfront and the rest in milestones, and the candidate started Phase 1 in March 2025. It is not counted here, but it explains why partners return.
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Tech-transfer office |
Monash Ventures |
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Licensed assets and licensees |
RB042, an inhaled splice-switching oligonucleotide that converts the RAGE receptor from a pro-inflammatory to an anti-inflammatory form, for COPD and related lung disease, held by RAGE Biotech |
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Spinouts and rounds |
RAGE Biotech Series A of A$29 million (November 2025), led by IP Group Australia and superannuation fund Hostplus, with Monash Ventures participating |
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The model that works |
A standing partnership with an IP commercialisation investor, plus pension capital |
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Note |
RAGE was co-founded with the University of Western Australia, Murdoch University and the Baker and Perron institutes; the lead programme is credited to Monash's Faculty of Medicine, Nursing and Health Sciences |
Monash earns its place on a single, well-documented round. Professor Merlin Thomas's RAGE biology and the company's splice-switching chemistry produced RB042, and the A$29 million Series A was sized to take it into the clinic. BioWorld reported in January 2026 that Phase 1 had begun, roughly two months after the money closed, which is fast by any academic spinout standard.
The detail worth noting is who wrote the cheque. Hostplus is a superannuation fund, and its presence alongside IP Group Australia shows how Australian institutions are pulling domestic pension money into early biotech. Monash also appears as a partner in the consortium behind WEHI's Ternarx (entry nine), and in September 2025 signed a memorandum with Korea's K-Bio Lab Hub to give Korean startups a Melbourne base.
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Tech-transfer office |
University of Tokyo TLO for licensing, with The University of Tokyo Edge Capital Partners (UTEC) as the affiliated venture investor |
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Licensed assets and licensees |
No qualifying drug-asset licence with disclosed terms found inside the window |
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Spinouts and rounds |
Celaid Therapeutics (University of Tokyo and University of Tsukuba): Series B first close of JPY 1.055 billion (October 2025) from venture investors and the Japan Agency for Medical Research and Development (AMED). TIME TRAVELER (Institute for Quantitative Biosciences): JPY 100 million (December 2025), bringing its total to about JPY 286 million |
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The model that works |
Volume. The university counted 743 related startups by the end of fiscal 2025, up 105 in a year, including 39 IPOs and 79 acquisitions |
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Note |
TIME TRAVELER also sells exosome-based health food and cosmetic materials alongside its cancer and anti-ageing drug work |
Tokyo ranks on companies, not licences. Celaid is built on Professor Satoshi Yamazaki's method for selectively expanding haematopoietic stem cells outside the body, and its lead product, CLD-001, aims to supply best-matched, bone-marrow-engrafting stem cells for transplant. The Series B is earmarked for advancing towards US clinical trials, and Osaka University Venture Capital joining UTEC in the round shows Japanese university funds now co-investing across campuses.
The Japanese-language release behind the TIME TRAVELER figure matters for accuracy. The company was set up in January 2024 on research by Professor Tetsu Akiyama, and the round is small. That is the honest picture of Japanese academic drug creation: enormous company formation, modest cheques, and very few out-licences priced in public.
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Tech-transfer office |
Kyoto University Innovation Capital (Kyoto iCAP) for venture creation; the Open Innovation Institute for industry agreements; iPS Academia Japan for the iPS cell patent estate |
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Licensed assets and licensees |
Anti-integrin alpha-v beta-6 antibody technology licensed to Link Therapeutics in December 2022 (before the window). Inside the window: an October 2025 incubation research agreement with Ciconia Bioventures to screen the university's drug discovery seeds for company creation |
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Spinouts and rounds |
Link Therapeutics Series B of JPY 850 million (July 2025), with ITOCHU Technology Ventures, Kyoto iCAP, MUFG's life science fund, SMBC Venture Capital and Kobe University Capital |
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The model that works |
Co-creation by the university's own investment arm, including an entrepreneurs-in-residence programme |
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Note |
Some English-language wires reported the Link round as JPY 8.5 billion. The Japanese original reads 8.5 oku yen, which is JPY 850 million. This list uses the corrected figure |
Link Therapeutics grew out of a finding by Masahiro Shiokawa's group in Kyoto's gastroenterology department that patients with ulcerative colitis carry autoantibodies against integrin alpha-v beta-6. The company is turning that into therapies that target pathogenic autoantibodies, and its Series B pulled in a trading house venture arm and two megabank funds alongside the university.
Kyoto iCAP is the engine behind the entry. Global University Venturing reports that nine companies co-created by the fund carry market capitalisations of at least JPY 10 billion, including the oncology developer Chordia Therapeutics. The Ciconia agreement suggests Kyoto is now trying to industrialise that process for drug discovery specifically, by inviting a venture builder to assess its pipeline of seeds before they are spun out.
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Tech-transfer office |
A*STAR industry innovation group; the 2025 licences were signed by its deputy chief executive for industry innovation |
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Licensed assets and licensees |
Two licences to HoneyBear Biosciences of Taiwan (12 March 2025): an exclusive licence to antibodies created at the A*STAR Singapore Immunology Network for antibody-radionuclide conjugates, and a non-exclusive licence to a multicistronic expression vector from the A*STAR Bioprocessing Technology Institute |
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Spinouts and rounds |
None counted. A*STAR also took equity in HoneyBear, its first investment in a Taiwanese biotech |
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The model that works |
Cross-border licence plus equity, pairing an Asian licensee's conjugation platform with A*STAR antibodies |
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Note |
English summaries of HoneyBear's later US$20 million Series A credit A*STAR as lead; the Chinese-language announcement names Taiwania Capital as lead. The licence terms remain undisclosed |
A*STAR's two licences sit behind a programme that is moving. HoneyBear says its lead antibody-radionuclide conjugate, HB001, is in late preclinical work with an IND filing targeted for the end of 2026, and its Series A brought total funding to US$34 million. For a government research agency, a licence that comes with an equity stake and a cross-strait partner is a notable shift from the classic option-and-royalty deal.
The rank reflects the method, not the institution's weight. A*STAR's best-known asset, the made-in-Singapore antibody-drug conjugate EBC-129, has progressed into Phase 1b dose expansion, but it has not been licensed out, and the 2022 Boehringer Ingelheim antibody deal falls before the window. On disclosed numbers alone, Singapore's flagship agency is quieter than its reputation.
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Tech-transfer office |
Business Development team, and WEHI Ventures, which manages the A$66 million 66ten seed fund |
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Licensed assets and licensees |
No new drug-asset licence with disclosed terms found inside the window |
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Spinouts and rounds |
Ternarx launched in June 2024 on A$15 million of Medical Research Future Fund support (a grant, not counted). In February 2026, Curie.Bio and WEHI Ventures invested to create a US spinout, Ternarx Bio, around its prostate cancer degrader programme; amount undisclosed. Further spinouts Nelcanen and Togglelux were formed in 2025 |
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The model that works |
An in-house seed fund that co-invests with global specialists |
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Note |
WEHI's best-known current asset, Pfizer's KAT6 inhibitor, entered Phase 3 in 2025 but was licensed well before the window |
WEHI is on this list for what its fund has started to do. Ternarx was the first Australian company dedicated to targeted protein degraders, born from a consortium of WEHI, the Children's Cancer Institute and Monash. When a US investor wanted its prostate programme, WEHI Ventures co-invested to spin the asset into a US entity while the Melbourne team kept equity and moved on to autoimmune targets. Forbes Australia quoted the chief executive as saying the lead asset now has its own funding in the US.
That is a template other institutes in the region can copy: keep the platform at home, let the first asset travel with a specialist investor, and retain a slice of both. The weakness, for ranking purposes, is that none of the money is disclosed.
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Tech-transfer office |
Joint licensing by the two institutes |
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Licensed assets and licensees |
An HSP subunit tuberculosis vaccine candidate in DDA adjuvant: technology transfer and commercialisation agreement with TechInvention Lifecare (November 2025). Terms undisclosed |
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Spinouts and rounds |
None |
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The model that works |
Co-development between a technology institute and a biology institute, licensed to a domestic vaccine developer |
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Note |
The only Indian entry that met the asset, licensee and date tests together |
India's academic system announces technology transfers frequently, but most are process know-how, diagnostics or reformulations, and many omit a date, a licensee or a defined asset. The Bhubaneswar tuberculosis vaccine agreement clears all three bars: a named candidate, a named licensee that will take it through development and validation, and a dated signing.
Its position at number ten is a statement about disclosure, not ambition. Other Indian items examined, including IIT Indore's engineered L-asparaginase transfer for leukaemia and CSIR-CDRI's 2024 co-development arrangement with Zydus on an osteoporosis drug for chronic kidney disease, either lacked terms or were structured as collaborations rather than licences. They are recorded here rather than counted.
The boundary rule asks that absences be stated. These institutions were searched in English and, where relevant, in Chinese, Japanese or Korean. Not finding a qualifying disclosure is not proof that none exists; it means none was public enough to verify.
For partnering teams meeting Asia-Pacific offices in Cologne this week, the practical questions follow from that. Does the office take equity, and has any of it been realised? Has a spinout ever licensed onward, and to whom? And will the office publish the terms? The institutions above can answer at least one of those with a number. Next year, the list will be longer if more of their peers can too.
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