- Cabaletta reported that its no-preconditioning clinical program for rese-cel is enrolling in the RESET-SLE and RESET-PV trials.
- Initial data from RESET-SLE in patients treated with a single weight-based dose of rese-cel without preconditioning are expected to be presented in 1H26, with durability data expected in 2H26.
- Dose-ranging durability data from RESET-PV without preconditioning are anticipated throughout 2026, supplementing previously presented low-dose pemphigus vulgaris data.
- Complete Phase 1/2 data from RESET-SLE, RESET-SSc, and RESET-MG evaluating rese-cel with preconditioning are expected to be presented in 1H26.
- Cabaletta expects to report initial clinical experience in 1H26 with rese-cel manufactured using the Cellares Cell Shuttle platform, with longer-term clinical data expected in 2H26.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Cabaletta Bio Inc. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001759138-26-000010), on March 23, 2026, and is solely responsible for the information contained therein.
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