Gene Therapy: Clinical Trials

5 trials for Gene Therapy, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

1 completed, 1 not yet recruiting, 1 recruiting, 1 terminated. 5 Phase 2, 4 Phase 1.

By phase and status

PhaseTrialsStatus
Phase 25Completed 1, Not yet recruiting 1, Recruiting 1, Terminated 1, Withdrawn 1
Phase 14Completed 1, Not yet recruiting 1, Recruiting 1, Terminated 1

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Trials (filtered) newest first · largest first

All 5 trials

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

TrialPhaseStatusSponsorEnrollmentStartUpdated
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47)
BFB-101 (AAV9-CBh-AP4B1) - HSP, Hereditary Spastic Paraplegia
Phase 1 / Phase 2Not yet recruitingBlackfinBio Ltd52025-08-012025-04-28
Intravitreal AAVCAGsCD59 for Advanced Dry Age-related Macular Degeneration (AMD) With Geographic Atrophy (GA)
Intravitreal AAVCAGsCD59, Intravitreal Sham Injection - Dry Age-related Macular Degeneration, Geographic Atrophy
Phase 2WithdrawnHemera Biosciences2021-07-312021-05-10
Dose-finding Study of SPK-8016 Gene Therapy in Patients With Hemophilia A to Support Evaluation in Individuals With FVIII Inhibitors
SPK-8016 - Adeno-Associated Virus (AAV), Blood Coagulation Disorder
Phase 1 / Phase 2CompletedSpark Therapeutics, Inc.42019-01-302024-02-23
Gene Therapy Study in Severe Hemophilia A Patients With Antibodies Against AAV5
Valoctocogene Roxaparvovec - Hemophilia A, Gene Therapy
Phase 1 / Phase 2TerminatedBioMarin Pharmaceutical32018-04-242025-08-22
Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning
autologous CD34+ cell transduced with G2SCID vector - Severe Combined Immunodeficiency, X Linked, Gene Therapy
Phase 1 / Phase 2RecruitingDavid Williams122018-02-262025-12-11

Narrower conditions

Blood Coagulation Disorders (2)  ·  Blood Coagulation Disorders, Inherited (2)  ·  Coagulation Protein Disorders (2)  ·  Genetic Diseases, Inborn (2)  ·  Hematologic Diseases (2)  ·  Hemophilia A (2)  ·  Hemorrhagic Disorders (2)  ·  Genetic Diseases, X-Linked (1)  ·  Geographic Atrophy (1)  ·  Hemostatic Disorders (1)  ·  Movement Disorders (1)  ·  Muscle Spasticity (1)  ·  Spastic Paraplegia, Hereditary (1)  ·  X-Linked Combined Immunodeficiency Diseases (1)

Broader conditions

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Genetic Diseases, Inborn (2)  ·  Hemic and Lymphatic Diseases (2)  ·  Cardiovascular Diseases (1)  ·  Central Nervous System Diseases (1)  ·  Congenital Abnormalities (1)  ·  Eye Diseases (1)  ·  Genetic Diseases, X-Linked (1)  ·  Hereditary Sensory and Motor Neuropathy (1)  ·  Heredodegenerative Disorders, Nervous System (1)  ·  Immune System Diseases (1)  ·  Immunologic Deficiency Syndromes (1)  ·  Infant, Newborn, Diseases (1)  ·  Macular Degeneration (1)  ·  Muscle Hypertonia (1)

Interventions

Valoctocogene Roxaparvovec (1)  ·  salicylhydroxamic acid (1)

Sponsors

BioMarin Pharmaceutical (1)  ·  BlackfinBio Ltd (1)  ·  David Williams (1)  ·  Hemera Biosciences (1)  ·  Spark Therapeutics, Inc. (1)

Countries

United States (3)  ·  South Africa (1)  ·  South Korea (1)  ·  Taiwan (1)  ·  United Kingdom (1)

Top investigators

Sung-Yun Pai, MD (1)  ·  Tiffany Chang, MD (1)

Results publications

PMID 41491634

NIH funding

2017 (1)