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Completed Phase 2 Interventional

Placebo Controlled, Randomized Safety and Efficacy Study of RC-1291 in Cancer Anorexia/Cachexia.

ClinicalTrials.gov ID: NCT00267358

Public ClinicalTrials.gov record NCT00267358. 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 Sep 3, 2026, 9:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

Anorexia and cachexia are devastating complications in late-stage cancer patients and is strongly associated with mortality in these patients. Activation of Ghrelin receptors have been demonstrated to stimulate appetite. RC-1291 HCl, by virtue of its ghrelin like activity and Growth Hormone releasing effects may have a dual role in the reversal of cancer induced anorexia and cachexia. This placebo controlled study will evaluate the safety and efficacy of RC-1291 HCl in cancer patients with anorexia and cachexia.

Study identification

NCT ID
NCT00267358
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
Not listed

Conditions and interventions

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
Oct 31, 2005
Primary completion
Sep 30, 2006
Completion
Sep 30, 2006
Last update posted
Sep 1, 2013

2005 – 2006

United States locations

U.S. sites
19
U.S. states
8
U.S. cities
16
Facility City State ZIP Site status
Palo Verde Hematology Oncology Ltd. Glendale Arizona 85304
Comprehensive Blood & Cancer Center Bakersfield California 93309
Pacific Oncology & Hematology Associates Encinitas California 92024
Pacific Oncology and Hematology Associates Encinitas California 92024
Advanced Medical Research Institute Fresno California 93710
Kenmar Clinical Research Los Angeles California 90057
Kenmar Research Institute Los Angeles California 90057
Sant Chawla, Inc. Santa Monica California 90403
PAB Clinical Research Brandon Florida 33511
Melbourne Internal Medicine Associates Melbourne Florida 32901
Osler Medical, Inc./ Osler Clinical Research Melbourne Florida 32901
Bay Area Oncology Tampa Florida 33607
Center for Cancer and Blood Disorders Bethesda Maryland 20817
Hematology Oncology Consultants, Inc. Columbus Ohio 43235
Charleston Cancer Center Charleston South Carolina 29406
South Carolina Oncology Associates Columbia South Carolina 29210
South Carolina Cancer Specialists Hilton Head Island South Carolina 29926
University of Texas Medical Texas Galveston Texas 77555
Multicare Health System Tacoma Washington 98405

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00267358, 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 Sep 1, 2013 · Synced Sep 3, 2026

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The complete protocol, eligibility criteria, and contact information for NCT00267358 live on ClinicalTrials.gov.

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