Proteus Syndrome: Clinical Trials

5 trials for Proteus Syndrome, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

2 completed, 1 active not recruiting, 1 no longer available, 1 recruiting. 1 Phase 1, 1 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 11Completed 1
Phase 21Active not recruiting 1

Follow Proteus Syndrome: new trials by email Literature Review of Proteus Syndrome trials Research Report on Proteus Syndrome

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
MK-7075 (Miransertib) in Proteus Syndrome
MK-7075 (miransertib) - Proteus Syndrome
Phase 2Active not recruitingNational Human Genome Research Institute (NHGRI)382022-05-202026-07-17
Dose Finding Trial of MK-7075 in Children and Adults With Proteus Syndrome
MK-7075 (miransertib) - Proteus Syndrome
Phase 1CompletedNational Human Genome Research Institute (NHGRI)62015-11-162022-06-30
Informed Consent for Whole Genome Sequencing: Ideals and Norms Referenced by Early Participants
Coronary Artery Disease, Proteus Syndrome
CompletedNational Human Genome Research Institute (NHGRI)302011-05-292018-07-26
Study of Proteus Syndrome and Related Congenital Disorders
Proteus Syndrome, PIK3CA Related Overgrowth Spectrum
RecruitingNational Human Genome Research Institute (NHGRI)15001994-04-272026-09-22
Expanded Access to Provide ARQ 092 for the Treatment of Overgrowth Diseases and/or Vascular Anomalies
ARQ 092 - Proteus Syndrome, PIK3CA-Related Overgrowth Spectrum (PROS)
No longer availableArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)2021-08-06

Narrower conditions

Growth Disorders (2)  ·  Abnormalities, Multiple (1)  ·  Congenital Abnormalities (1)  ·  Coronary Artery Disease (1)  ·  Genetic Diseases, Inborn (1)  ·  Hereditary Sensory and Autonomic Neuropathies (1)  ·  Hyperparathyroidism 2 (1)

Broader conditions

Bone Diseases (5)  ·  Bone Diseases, Developmental (5)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5)  ·  Hamartoma (5)  ·  Hamartoma Syndrome, Multiple (5)  ·  Limb Deformities, Congenital (5)  ·  Musculoskeletal Abnormalities (5)  ·  Musculoskeletal Diseases (5)  ·  Neoplasms (5)  ·  Neoplasms, Multiple Primary (5)  ·  Abnormalities, Multiple (4)  ·  Congenital Abnormalities (4)  ·  Pathologic Processes (2)  ·  Pathological Conditions, Signs and Symptoms (2)  ·  Arterial Occlusive Diseases (1)

Interventions

Miransertib (3)

Sponsors

National Human Genome Research Institute (NHGRI) (4)  ·  ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA) (1)

Countries

United States (4)

Top investigators

Leslie G Biesecker, M.D. (3)  ·  Barbara B Biesecker (1)

Results publications

PMID 34649967, PMID 30803705, PMID 35839129, PMID 42224880, PMID 42289769