Study of MRM-3379 in Male Participants With Fragile X Syndrome (BLOOM)

Recruiting Phase 2 Interventional Study
Fragile X Syndrome
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
13 – 45
Sex
Male
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
Mirum Pharmaceuticals, Inc. · Industry
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About This Trial
This study is a multicenter, double-blind, randomized, placebo-controlled study to assess the safety and tolerability of 3 doses of MRM-3379 in male participants with Fragile X Syndrome ages 16 to 45 (inclusive). In addition, a parallel cohort of participants ages 13 to \<16 will receive open-label MRM-3379. All participants will participate for 12 weeks of treatment. The study is also intended as…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Willing and able to provide signed informed consent/assent. Where local regulations permit inclusion of participants deemed unable to provide informed consent, a legally authorized representative must provide informed consent on the participant's behalf, and the participant mu…
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