OnCo
ideasIdea

A fast IND-enabling fund that pays for toxicology and manufacturing in eight weeks

The studies needed before a first human trial cost a few million and no grant pays for them. A dedicated fund would decide in weeks and take a small share of any future revenue.

A revolving fund, capitalised by philanthropy and public money, that pays for GLP toxicology, CMC development, formulation and regulatory writing for academic oncology candidates that have passed independent replication of the key efficacy result. Decisions in eight weeks by a standing expert panel; awards of $2 to $8 million; in return the fund takes a low single-digit royalty or a share of licensing revenue, recycled into the fund. Structured like the Wellcome Trust's Seeding Drug Discovery or the Michael J. Fox Foundation's therapeutic pipeline programme, but oncology-focused and paired with the translational institutes. Most academic assets stall exactly here because IND-enabling work is neither science (so not fundable by grants) nor de-risked enough for companies.

Hypothesis
A fund of $100 million enables at least twenty academic oncology candidates to file INDs within four years, of which at least a quarter are licensed or reach phase 2, with royalty and licensing returns covering more than a third of disbursements over ten years.
Rationale
Seeding Drug Discovery and similar translational funds report that a substantial fraction of supported programmes attract industry partners; the Cystic Fibrosis Foundation's programme returned billions from a comparable model. Speed matters because academic teams disperse and competitors move on during multi-year funding delays.
What would test it
Capitalise a pilot at $20 million, fund ten candidates with the eight-week process, and track INDs filed, licensing and time-to-decision against a historical academic cohort.
Maturity
speculative
Who has to act
philanthropy
Cost to try
Medium ($1M to $50M)
Years to first evidence
3
Bottlenecks it attacks

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