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Results for “LMNA Related Disorders”

7 trials

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Showing 7 of 7 results

Early research (Phase 1)Study completedNCT05286281
What this trial is testing

Evaluate The Pharmacokinetics, Excretion, Mass Balance and Metabolism of PF-07265803

Who this might be right for
Healthy
Pfizer 6
Testing effectiveness (Phase 2)Study completedNCT02057341
What this trial is testing

ARRY-371797 in Patients With LMNA-Related Dilated Cardiomyopathy

Who this might be right for
LMNA-Related Dilated Cardiomyopathy
Pfizer 12
Not applicableNo Longer AvailableNCT05154851
What this trial is testing

HBCMD01- Expanded Access for the Treatment of Congenital Muscular Dystrophy.

Who this might be right for
Congenital Muscular Dystrophy Due to Lamin A/C Mutation
Hope Biosciences Research Foundation
Testing effectiveness (Phase 2)Study completedNCT02351856
What this trial is testing

A Rollover Study of ARRY-371797 in Patients With LMNA-Related Dilated Cardiomyopathy

Who this might be right for
LMNA-Related Dilated Cardiomyopathy
Pfizer 8
Not applicableLooking for participantsNCT05394506
What this trial is testing

Modifying Factors in Striated Muscle Laminopathies

Who this might be right for
LaminopathiesEmery Dreifuss Muscular Dystrophy 2LMNA-Related Congenital Muscular Dystrophy+1 more
Institut National de la Santé Et de la Recherche Médicale, France 40
Not applicableNot Yet RecruitingNCT07412028
What this trial is testing

Identification of Women With Severe Insulin Resistant Syndromes of Genetic Origin Among Patients With "Classic" Polycystic Ovary Syndrome (PCOS)

Who this might be right for
Polycystic Ovary SyndromeFamilial Partial LipodystrophyLMNA (LaMin Nuclear A) Related Disorders
Assistance Publique - Hôpitaux de Paris 81
Not applicableLooking for participantsNCT01403402
What this trial is testing

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Who this might be right for
Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) DeficiencyAlpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)+49 more
Cure CMD
4,000