HomeTrialNCT06924970
NCT06924970Phase 2RECRUITING

A Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD)

Study Summary

The main purpose of this study is to compare the effect of tebapivat versus placebo on anemia and to detect a dose-response for hemoglobin (Hb) response in participants with SCD.

View on ClinicalTrials.gov ↗
Study Details
Enrollment56 participants
Primary Completion
Lead SponsorAgios Pharmaceuticals, Inc.
Data Retrieved2026-04-11 02:52:46.814983+00:00
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 2 trials begin testing efficacy in a larger patient group (100–300). This is often where biotech binary events occur — positive Phase 2 data can significantly advance a company's pipeline narrative, while failures can be terminal for a program.

Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 56 participants
Sponsor Catalyst Profile

Agios Pharmaceuticals (AGIO) is the sponsoring company for this trial. BiotechSign currently grades this company A (88/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

Not financial advice. BiotechSign data is sourced from ClinicalTrials.gov, SEC EDGAR, and other public databases for research and informational purposes only. It does not constitute investment recommendations. Always do your own due diligence before making investment decisions.