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Obsidian says $324m cash covers amsoki-cel study data due late 2027

The cell therapy developer's reported funding extends into the second half of 2028, beyond its planned topline readout, as early melanoma data come from a small group of patients.

12 Nov 2026 · Obsidian Therapeutics, Inc. OBX · Company news

Obsidian Therapeutics says its balance sheet should last beyond the next major milestone for amsoki-cel. The company reported $324.4 million in cash with its third-quarter results on 12 November, and said this funds operations into the second half of 2028. It expects topline data from its Agni-01 study by the end of 2027, so the stated runway extends past that readout.

The quarterly net loss was $50.7 million. Obsidian did not give further spending guidance in the material available to CompePharma, and no revenue figures were provided.

The financials came with updated clinical data for amsoki-cel, an engineered tumour-infiltrating lymphocyte therapy, presented at the SITC meeting. In melanoma that had stopped responding to checkpoint inhibitors, the company reported that roughly two-thirds of 15 patients (67%) had a tumour response. Median time before disease progression or death was 8.3 months. Details on the patients' prior treatments and on follow-up length were not provided.

On tolerability, Obsidian pooled data from 37 patients and reported no cases of ICANS, no dose-limiting toxicities and no treatment-related deaths. Enrolment in Agni-01, the cohort intended to support a registration filing, is due to finish by the end of the first quarter of 2027. The efficacy and safety figures are company-reported and come from a small sample, so they are early signals rather than confirmatory evidence.

Why it matters

  • Reported cash of $324.4m is said to last into the second half of 2028, giving Obsidian funding beyond its planned end-2027 topline readout.
  • Enrolment completion by end of Q1 2027 and topline data by end of 2027 set the earliest window for any regulatory filing discussions.
  • The 67% response figure rests on 15 patients and a company announcement, so commercial planners should treat it as preliminary.
  • The clean safety record in 37 patients will be tested as the registration cohort grows.

Company's press release (SEC filing): Obsidian Therapeutics, Inc. ↗

Written by CompePharma's editorial system from the company's filing; claims are the company's. AI-assisted; check the source before acting. Not investment advice.

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