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Cancer CachexiaPhase 2NCT00267358

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

A Phase 2 study testing RC-1291 HCl in people with Cancer Cachexia, run by Helsinn Therapeutics (U.S.), Inc at 19 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer Cachexia
What is being tested?
RC-1291 HCl
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
Not given
Where
19 sitesUnited States
Study dates
Nov 2005to Oct 2006
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Community-dwelling patients ≥ 18 years of age with incurable,histologically diagnosed cancer.
  • Involuntary loss of body weight of ≥ 5 % within the past 6 months

Who cannot join

  • Presently hospitalized or in a nursing care facility.
  • Inability to increase food intake from secondary causes.
  • Liver disease
  • If female-pregnant, breast-feeding or of childbearing potential.

Trial locations and contacts

19 sites in 1 country.

19 sites in 1 country

United States19 sites
  • Comprehensive Blood & Cancer Center

    Bakersfield, California, 93309

  • Center for Cancer and Blood Disorders

    Bethesda, Maryland, 20817

  • PAB Clinical Research

    Brandon, Florida, 33511

  • Charleston Cancer Center

    Charleston, South Carolina, 29406

  • South Carolina Oncology Associates

    Columbia, South Carolina, 29210

  • Hematology Oncology Consultants, Inc.

    Columbus, Ohio, 43235

  • Pacific Oncology & Hematology Associates

    Encinitas, California, 92024

  • Pacific Oncology and Hematology Associates

    Encinitas, California, 92024

  • Advanced Medical Research Institute

    Fresno, California, 93710

  • University of Texas Medical Texas

    Galveston, Texas, 77555

  • Palo Verde Hematology Oncology Ltd.

    Glendale, Arizona, 85304

  • South Carolina Cancer Specialists

    Hilton Head Island, South Carolina, 29926

  • Kenmar Clinical Research

    Los Angeles, California, 90057

  • Kenmar Research Institute

    Los Angeles, California, 90057

  • Melbourne Internal Medicine Associates

    Melbourne, Florida, 32901

  • Osler Medical, Inc./ Osler Clinical Research

    Melbourne, Florida, 32901

  • Sant Chawla, Inc.

    Santa Monica, California, 90403

  • Multicare Health System

    Tacoma, Washington, 98405

  • Bay Area Oncology

    Tampa, Florida, 33607

Other trials in United States

About this study

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.

Conditions
Cancer Cachexia
Being tested
RC-1291 HCl, Placebo

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RC-1291 HClDrug

  • PlaceboDrug

Study groups in NCT00267358
Study groupRoleWhat they receive
RC-1291 HClActive comparator50 mg
Receives: Drug: RC-1291 HCl
PlaceboPlacebo comparatorNot described
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Body weight

  2. Lean body mass

  3. Functional performance

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Dec 2005 (estimated)
  2. Study startNov 2005
  3. Primary completionOct 2006
  4. Study completionOct 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
IDs, dates and publications
ClinicalTrials.gov ID
NCT00267358
Sponsor's protocol ID
RC-1291-205
Status last verified
Aug 2013
First submitted
19 Dec 2005
Last updated
2 Sep 2013
Results posted
No

Publications

  • Garcia JM, Boccia RV, Graham CD, Yan Y, Duus EM, Allen S, Friend J. Anamorelin for patients with cancer cachexia: an integrated analysis of two phase 2, randomised, placebo-controlled, double-blind trials. Lancet Oncol. 2015 Jan;16(1):108-16. doi: 10.1016/S1470-2045(14)71154-4. Epub 2014 Dec 16.

    PubMed 25524795

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing RC-1291 HCl in people with Cancer Cachexia, run by Helsinn Therapeutics (U.S.), Inc at 19 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Sep 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 19 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body weight. The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00267358, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Sep 2013.

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