Drugs / RCT2100
last change Aug 2026 re-read 9 days ago

RCT2100

Messenger RNA (mRNA)

Developed for
cystic fibrosis
Investigated by
ReCode Therapeutics

Trials 1

20252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2 NCT06237335 Feb 2024 → Aug 2026 overdue cystic fibrosis ReCode Therapeutics Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2025-11-17 ReCode Therapeutics Regulatory ReCode Therapeutics Initiates Enrollment of Phase 2 Clinical Trial of RCT2100 in Combination with Ivacaftor for the Treatment of Cystic Fibrosis recodetx.com ↗
2025-03-25 ReCode Therapeutics Regulatory ReCode Therapeutics Receives U.S. FDA Orphan Drug Designation for RCT2100 for the Treatment of Cystic Fibrosis recodetx.com ↗
2024-09-26 ReCode Therapeutics Results ReCode Therapeutics Presents Preclinical Data from its Cystic Fibrosis Program at the 2024 North American Cystic Fibrosis Conference (NACFC) in Boston recodetx.com ↗
In the studies, RCT2100, an inhaled mRNA-based therapy, successfully restored CFTR function in patient-derived cells in vitro and improved mucociliary clearance, which is critical for improving patient outcomes, in a ferret model of CF lung disease.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as RCT2100 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06237335 ↗
Modality Messenger RNA (mRNA) “RCT2100 (CFTR mRNA)” NCT06237335 ↗
Route Inhaled “administered via oral inhalation using nebulizer” NCT06237335 ↗