exagamglogene autotemcel: Clinical Trials

9 trials of exagamglogene autotemcel, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

3 recruiting, 2 active not recruiting, 2 completed, 1 enrolling by invitation. 7 Phase 3, 3 Phase 2, 1 Early Phase 1, 1 Phase 1.

By phase and status

PhaseTrialsStatus
Phase 37Active not recruiting 2, Completed 2, Enrolling by invitation 1, Recruiting 1, Withdrawn 1
Phase 23Completed 2, Recruiting 1
Early Phase 11Recruiting 1
Phase 11Recruiting 1

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Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Evaluation of Efficacy and Safety of a Single Dose of Exa-cel in Participants With Severe Sickle Cell Disease, βS/ βC Genotype
Exa-cel - Sickle Cell Disease
Phase 3WithdrawnVertex Pharmaceuticals Incorporated2027-07-312026-03-25
A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CTX001 in Healthy Adults.
CTX001 With and Without Iron, CTX001 With Iron, CTX001 Multiple Dose - Anemia, Iron Deficiencies
Early Phase 1RecruitingCajal Therapeutics Inc.722026-06-012026-06-12
An Optimised GA Interventional Trial (Opti-GAIN) to Test if Treatment With CTx001 is Safe and Works for People With Geographic Atrophy (GA)
CTx001 - Geographic Atrophy Secondary to Age-related Macular Degeneration
Phase 1 / Phase 2RecruitingComplement Therapeutics752025-12-302026-10-16
Evaluation of Efficacy and Safety of a Single Dose of CTX001 in Participants With Transfusion-Dependent β-Thalassemia and Severe Sickle Cell Disease
CTX001 - Beta-Thalassemia, Thalassemia
Phase 3RecruitingVertex Pharmaceuticals Incorporated262022-08-022026-03-23
Evaluation of Safety and Efficacy of CTX001 in Pediatric Participants With Transfusion-Dependent β-Thalassemia (TDT)
CTX001 - Beta-Thalassemia, Thalassemia
Phase 3Active not recruitingVertex Pharmaceuticals Incorporated162022-05-032026-07-01
Evaluation of Safety and Efficacy of CTX001 in Pediatric Participants With Severe Sickle Cell Disease (SCD)
CTX001 - Sickle Cell Disease, Hydroxyurea Failure
Phase 3Active not recruitingVertex Pharmaceuticals Incorporated132022-05-022026-07-01
A Long-term Follow-up Study in Participants Who Received CTX001
CTX001 - Beta-Thalassemia, Thalassemia
Phase 3Enrolling by invitationVertex Pharmaceuticals Incorporated1602021-01-202026-08-11
A Safety and Efficacy Study Evaluating CTX001 in Subjects With Severe Sickle Cell Disease
Exa-cel - Sickle Cell Disease, Hematological Diseases
Phase 2 / Phase 3CompletedVertex Pharmaceuticals Incorporated632018-11-272026-09-16
A Safety and Efficacy Study Evaluating CTX001 in Participants With Transfusion-Dependent β-Thalassemia
CTX001 - Beta-Thalassemia, Thalassemia
Phase 2 / Phase 3CompletedVertex Pharmaceuticals Incorporated592018-09-142025-12-17

Conditions studied

Hematologic Diseases (6)  ·  Hemoglobinopathies (6)  ·  Anemia, Sickle Cell (5)  ·  Genetic Diseases, Inborn (4)  ·  Thalassemia (4)  ·  beta-Thalassemia (4)  ·  Anemia (1)  ·  Iron Deficiencies (1)  ·  Renal Insufficiency, Chronic (1)

Sponsors

Vertex Pharmaceuticals Incorporated (7)  ·  Cajal Therapeutics Inc. (1)  ·  Complement Therapeutics (1)

Countries

United States (7)  ·  Germany (6)  ·  Italy (6)  ·  United Kingdom (6)  ·  Canada (4)  ·  Belgium (2)  ·  Australia (1)  ·  France (1)  ·  Saudi Arabia (1)

Top investigators

Aarthy Joseph, Dr (1)

Results publications

PMID 33283989, PMID 34175041, PMID 40857358, PMID 40862696, PMID 42252696, PMID 42274009, PMID 32873924, PMID 36123234, PMID 36860093, PMID 36975201, PMID 38657265, PMID 38661449, PMID 38866240

NIH funding

2023 (1)