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ACTIVE NOT RECRUITING
NCT06597396
PHASE2

Study to Investigate the Efficacy of Abrocitinib in Adult Participants With Severe Fatigue From Post COVID Condition/Long COVID

Sponsor: Beth Israel Deaconess Medical Center

View on ClinicalTrials.gov

Summary

The primary purpose of this phase 2a study is to compare the efficacy of abrocitinib to placebo in improving severe fatigue in non-hospitalized adults with symptomatic Post-COVID Condition (PCC) (also called Long COVID). We are also interested in learning if abrocitinib is effective in improving overall health status in people suffering from severe fatigue from PCC. Eligible participants with a confirmed history of COVID19 infection who also have PCC according to the World Health Organization definition, will be randomized to receive abrocitinib at a dose of 50 mg, 100 mg, or placebo by mouth daily for 12 weeks (84 days).

Official title: A Phase 2a Randomized, Dose Ranging, Double-Blind, 3-Arm Study to Investigate Orally Administered Abrocitinib Compared With Placebo in Non-Hospitalized Symptomatic Adult Participants With Severe Fatigue From Post COVID Condition

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

46

Start Date

2024-12-27

Completion Date

2026-09-30

Last Updated

2025-12-17

Healthy Volunteers

No

Interventions

DRUG

Abrocitinib

50 mg tablets

DRUG

Placebo

Tablets

Locations (1)

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States