Acromegaly Clinical Trial
Official title:
Efficacy and Safety of Oral Octreolin™ in Patients With Acromegaly Who Are Currently Receiving Parenteral Somatostatin Analogs
MYCAPSSA™ (formerly Octreolin™) is a proprietary oral form of the approved injectable medical product octreotide used to treat acromegaly. This study will evaluate the efficacy and safety of MYCAPSSA™ treatment in patients with acromegaly.
The study consisted of 2 periods, a Core Treatment Period of up to 7 months and an optional
Extension Treatment Period of up to 6 months, for a total study duration of up to 13 months.
The Core Treatment Period consisted of 2 phases, a Dose Escalation Phase of at least 2
months to identify the therapeutic dose for each study participant and a Fixed Dose Phase of
2 to 5 months during which the therapeutic dose was maintained.
Participants were eligible to enter the Fixed Dose Phase of the Core Treatment Period if
they were clinically and biochemically controlled. The same criteria were used to allow
entry into the voluntary 6-month Extension Treatment Period.
The Core Treatment Period of the study was completed if the participant had at least 2
months of treatment in the Fixed Dose Phase and a total treatment duration of at least 7
months. Participants who elected to continue into the Extension Treatment Period maintained
their therapeutic dose during this period. At the end of the study (after the last dose of
MYCAPSSA in either the Core Treatment Period or the Extension Treatment Period), there was a
2-week follow-up period for safety assessments.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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