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A Phase 2/3 Study in Adult and Pediatric Participants With SCD

Phase 2
Active, not recruiting
Conditions
Sickle Cell Disease
Interventions
Registration Number
NCT05431088
Lead Sponsor
Pfizer
Brief Summary

The purpose of this study is to evaluate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of osivelotor.

Detailed Description

This is a three-part, multicenter, Phase 2/3 study of orally administered osivelotor in participants with sickle cell disease (SCD).

Part A will evaluate the safety, tolerability, and efficacy of osivelotor in adult participants with SCD to determine an optimal dose.

Part B will evaluate the efficacy of osivelotor versus placebo in adult and adolescent participants with SCD for 48 weeks.

Part C will evaluate the pharmacokinetics (PK) and safety of single and multiple doses (MD) of open-label single arm osivelotor administered to pediatric participants.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
429
Inclusion Criteria

Part A, Part B, and Part C:

  • Male or female with SCD
  • Participants with stable Hb value as judged by the Investigator
  • For participants taking hydroxyurea and/or L-glutamine, the dose must be stable for at least 90 days prior to signing the ICF or assent and with no anticipated need for dose adjustments during the study in the opinion of the Investigator.

Part B:

  • Participants with SCD ages 12 to 65 years, inclusive
  • Participants with more than or equal to 2 and ≤ 10 VOCs within 12 months of Screening.
Exclusion Criteria

Part A, Part B, and Part C:

  • Participants who had more than 10 VOC within 12 months of screening
  • Female participant who is breastfeeding or pregnant
  • Participants who receive RBC transfusion therapy regularly or received an RBC transfusion ---for any reason within 90 days of Day 1
  • Participants hospitalized for sickle cell crisis or other vaso-occlusive event within 14 days of signing the ICF

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Part COsivelotor100 mg dose in cohort C1, dose level for cohorts C2 to C4 to be determined based on emerging data
Part AOsivelotorInitially, participants will be randomized 1:1 to 100 mg and 150 mg daily. Upon review of the 150 mg safety data from at least 6 participants, there will be 1:1:1 randomization: 100 mg, 150 mg, and up to 200 mg. Participants will then receive maintenance once daily doses through Week 12.
Part BOsivelotorFollowing the selection of the optimal safe and effective dose from Part A of the study, Part B of the study will assess the efficacy and safety of 48 weeks of the optimal dose, compared to placebo
Primary Outcome Measures
NameTimeMethod
Part AThrough week 12

Number of adult participants with change from baseline in hemoglobin (Hb) through week 12 as measured by change in osivelotor concentrations from baseline or percentage change from baseline of clinical measures of anemia Hb and hemolysis (including indirect bilirubin, reticulocytes and lactate dehydrogenase).

Part BThrough week 48

Co-primary endpoints: Hb response (increase from baseline of \>1 g/dL) at Week 48 (based on average of Hb levels at Week 40 and Week 48) and the Annualized rate of VOC through end of Week 48.

A VOC is defined as an acute episode of pain that:

* Has no medically determined cause other than a vaso-occlusive event, and

* Results in a visit to a medical facility (hospitalization, emergency department, urgent care center, outpatient clinic, or infusion center), and

* Requires parenteral narcotic agents, parenteral nonsteroidal anti-inflammatory drugs (NSAIDs), or an increase in treatment with oral narcotics.

Complicated VOCs of acute chest syndrome (ACS), hepatic sequestration, splenic sequestration, priapism, and dactylitis that meet the requirements listed above will be included in this co-primary endpoint.

Part CThrough Week 2

Assess the PK AUC0-last, AUC0-inf, and Cmax after single dose of osivelotor in whole blood and plasma.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (24)

Smilow Cancer Hospital

🇺🇸

New Haven, Connecticut, United States

Children's National Hospital

🇺🇸

Washington, District of Columbia, United States

Edward Jenner Research Group Center LLC

🇺🇸

Plantation, Florida, United States

Pediatric Hematology / Oncology a division of Kidz Medical services

🇺🇸

West Palm Beach, Florida, United States

Sonar Clinical Research

🇺🇸

Atlanta, Georgia, United States

Alpha Clinical Research Georgia

🇺🇸

Dunwoody, Georgia, United States

University of Illinois at Chicago Clinical Research Center

🇺🇸

Chicago, Illinois, United States

LSU Health Baton Rouge-North Clinic

🇺🇸

Baton Rouge, Louisiana, United States

University Medical Center New Orleans

🇺🇸

New Orleans, Louisiana, United States

Mississippi Center for Advanced Medicine

🇺🇸

Madison, Mississippi, United States

Scroll for more (14 remaining)
Smilow Cancer Hospital
🇺🇸New Haven, Connecticut, United States

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