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Study details
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A Study to Evaluate How Well Etavopivat Works in People With Sickle Cell Disease

Novo Nordisk A/S
NCT IDNCT06612268ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

408

Study length

about 4.1 years

Ages

12+

Locations

49 sites in AL, AR, AZ +24

About this study

Researchers are testing whether etavopivat reduces the number of vaso-occlusive crises (sickle cell pain crises) caused by blood vessel blockages in adults and adolescents with sickle cell disease. The trial will also evaluate how well etavopivat can reduce organ damage, improve exercise tolerance, and decrease fatigue in people with sickle cell disease. Participants will either receive etavopivat or a placebo. Which treatment they get is decided randomly. Etavopivat is a new medicine being tested in other studies as well.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Etavopivat
  • 2.Take Placebo
PhasePhase 3

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Secondary: Change in distance travelled during the 6-minute walking test (6MWT), Change in standardised T-score on the Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue 7a Scale, Participants achieving the threshold for clinically meaningful change (yes/no) in 6MWT, Participants achieving the threshold for clinically meaningful change (yes/no) in PROMIS fatigue scale 7a