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A Study of Mitapivat in Participants With Sickle Cell Disease and Nephropathy

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NCT06286046 · readout ≤ 284 d

Sponsored by Agios Pharmaceuticals, Inc. (industry) · AGIO — their whole pipeline →.

Phase
Phase 2
Status
Withdrawn
Study type
Interventional
Design
Na · None · Treatment
Enrollment
0actual

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Withdrawn prior to study start per sponsor decision. No patients were enrolled.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartMar 2026estimatedWhen the study began enrolling
Primary completionMay 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2028estimatedThe whole study's end, after follow-up
First posted2024-02-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Sickle Cell Disease
  • Nephropathy

Intervention

  • Drug: Mitapivat — also filed as AG-348, Mitapivat sulfate, AG-348 sulfate hydrate

Primary outcome

what the primary-completion date above is the date OF
Percentage of Participants With Albumin Creatinine Ratio (ACR) Response
measured Baseline up to 6 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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