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Not listed Phase 3 Interventional Results available

Efficacy and Safety of Octreotide Capsules (MYCAPSSA) in Acromegaly

ClinicalTrials.gov ID: NCT03252353

Public ClinicalTrials.gov record NCT03252353. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 6:40 PM EST

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Official title

A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate Efficacy and Safety of Octreotide Capsules in Patients Who Demonstrated Biochemical Control on Injectable Somatostatin Receptor Ligands (SRL) Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Octreotide capsule is a novel, orally-administered formulation of the commercially-available injectable drug octreotide. In a recent phase 3 trial, oral octreotide capsules demonstrated maintenance of biochemical response up to 13 months in the majority of patients with acromegaly previously managed with somatostatin analog injections (reference below).

Study identification

NCT ID
NCT03252353
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Chiasma, Inc.
Industry
Enrollment
56 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 1, 2017 (Actual)
Primary completion
Jun 13, 2019 (Actual)
Completion
May 2022 (Estimated)
Last update posted
Nov 23, 2020

2017 – 2022

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Keck Medical Center of University of Southern California Los Angeles California 90033 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
UCLA Medical Center Los Angeles California 90095 —
Stanford University School of Medicine Palo Alto California 94304 —
University of Colorado Aurora Colorado 80045 —
The Emory Clinic Atlanta Georgia 30322 —
John H. Stroger Jr. Hospital of Cook County Chicago Illinois 60612 —
Johns Hopkins University Clinical Trials Unit Baltimore Maryland 21287 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Washington University School of Medicine St Louis Missouri 63110 —
Columbia University Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Cleveland Clinic Cleveland Ohio 44195 —
Ohio State University Columbus Ohio 43203 —
Oregon Health and Science University Portland Oregon 97239 —
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107 —
Allegheny Endocrinology Associates Pittsburgh Pennsylvania 15212 —
Baylor College of Medicine Houston Texas 77030 —
Huntsman Cancer Hospital Salt Lake City Utah 84108 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03252353, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 23, 2020 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03252353 live on ClinicalTrials.gov.

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