A Study of IMR-687 in Adult Participants With Sickle Cell Anemia (Homozygous HbSS or Sickle-β0 Thalassemia)

PHASE2CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

January 26, 2018

Primary Completion Date

August 28, 2020

Study Completion Date

August 28, 2020

Conditions
Sickle Cell Disease
Interventions
DRUG

IMR-687

Oral administration of IMR-687 once daily with or without HU.

DRUG

Placebo

Oral administration of placebo once daily with or without HU.

Trial Locations (13)

29425

Medical University of South Carolina, Charleston

33021

Foundation for Sickle Cell Disease Research, Hollywood

60612

University of Illinois, Chicago

60644

Loretto Hospital, Chicago

76508

Baylor Scott & White Health, Temple

94609

UCSF Benioff Children's Hospital Oakland, Oakland

06030

University of Connecticut Health Center, Farmington

B18 7QH

Sandwell & West Birmingham Hospital, Birmingham

BS2 8ED

Bristol Haematology and Oncology Centre, Bristol

E1 1BB

Royal London Hospital, London

NW1 2PG

University College London Hospital, London

SE1 9RT

Guy's Hospital, London

OX3 7LE

Oxford Cancer & Haematology Centre, The Churchill Hospital, Oxford

All Listed Sponsors
collaborator

Imara, Inc.

INDUSTRY

lead

Cardurion Pharmaceuticals, Inc.

INDUSTRY