Adicet Bio posts September 2026 investor presentation with program timelines
Adicet Bio posted a September 2026 investor presentation to its website and furnished it as Exhibit 99.1 to a Form 8-K. The deck covers its prula-cel autoimmune program, its ADI-212 solid tumor candidate and its in vivo CAR-T pipeline, and sets out expected clinical and regulatory milestones.
Key points
- ADI-212 has an IND cleared in the US, with first-patient dosing anticipated in 4Q26 and clinical data expected in 1H27 and 2H27.
- Prula-cel clinical data cited in the deck has a cut-off date of August 31, 2025 and covers 7 patients (5 LN and 2 SLE) with follow-up of 2-9 months.
- The filing describes a CRISPR license for ADI-212 gene-editing technology, with CRISPR holding an opt-in right to a 50/50 cost and profit split.
The filing
Written by AI on Nov 9, 2026, 8:53 AM ET, from this filing only. Written later: this filing was briefed after the fact, when past filings were added to the site, so the brief may be read with hindsight; the filing itself is the record of what was known on September 08, 2026.
Briefs are written by AI from the filing text and can contain mistakes — open the filing before acting on anything. Impact (1-5) and tone are the AI's reading of the filing for shareholders, not a price forecast. Not investment advice.