Study of BBP-418 in Patients With LGMD2I (NCT04800874) | Clinical Trial Compass
Active — Not RecruitingPhase 2
Study of BBP-418 in Patients With LGMD2I
United States14 participantsStarted 2021-02-18
Plain-language summary
BBP-418 is being developed for the treatment of patients with Limb-Girdle Muscular Dystrophy Type 2I (LGMD2I). This is an open label study to determine the safety and tolerability of ascending dose levels of BBP-418 in the treatment of ambulatory and non-ambulatory patients with LGMD2I for which no approved therapy currently exists.
Who can participate
Age range12 Years – 55 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Have a body weight \>30 kg
* Have a genetically confirmed diagnosis of LGMD2I and be clinically affected (defined as demonstrating clinical weakness on bedside evaluation in either a limb-girdle pattern, or in a distal extremity)
* Able to complete the 10-meter walk test in ≤ 12 seconds unaided ("moderate disease") or are with "severe disease"/non-ambulatory as defined by being unable to complete the 10-meter walk unaided in \>12 seconds
* Willing to use an adequate method of contraception from time of consent through 12 weeks after last dose
* Previous enrolment in the Natural History study MLB-01-001
Exclusion Criteria:
* Evidence of clinically significant concomitant disease, including:
* Any history of a gastrointestinal condition, including surgeries, which may affect absorption after oral administration
* Any significant concomitant medical condition, including cardiac, pulmonary, renal, hepatic or endocrine disease other than that associated with LGMD2I
* Any condition other than LGMD2I requiring therapy with prescription medicine (medication for common and mild concomitant conditions may be permitted after consultation with the PI)
* Any other laboratory, vital sign, ECG abnormality, or clinical history or finding that, in the investigator's opinion, is likely to unfavorably alter the risk-benefit of study participation, confound study results, or interfere with study conduct or compliance
* If pregnant and/or breastfeeding or plannin…
What they're measuring
1
Incidence of treatment-emergent adverse events (TEAEs) that lead to dose decrease or discontinuation