The Role of Ghrelin in Cancer Cachexia

Phase 2

Terminated

• Conditions: Cancer Cachexia
• Interventions: Drug: Placebo; Drug: Anamorelin HCl

• Registration Number: NCT01505764
• Lead Sponsor: VA Office of Research and Development

Brief Summary

Cancer is often coupled with a condition called cachexia. In this condition, individuals continue to lose weight and lean body mass, which means their muscles are getting smaller and weaker. Studies have shown that cancer patients who are losing weight often are responding poorly to chemotherapy, are at greater risk of infection and have a reduced life expectancy. Also, people may not want to eat. To date, there are no approved treatments available for this condition.

This study is going to study the benefits of the use of the study drug, Anamorelin hydrochloride (HCl) in treatment or prevention of cachexia associated with cancer. Studies done before with the study drug have shown that the drug can help the cachectic condition. The purpose of this research study is to evaluate the effectiveness of Anamorelin HCl compared to placebo on body composition (amount of cell mass, fat, muscle, etc.) including measurements of body potassium and nitrogen stores.

In addition to the above, the study will also assess the effect of the study drug on handgrip strength, body weight, lean muscle mass, quality of life, appetite \& food intake, certain blood markers, energy expenditure (the amount of energy participants burn), functional performance, safety and tolerability of Anamorelin HCl.

Detailed Description

Subjects enrolled in the study will be randomly chosen to receive either Anamorelin HCL at a dose of 100 mg per day for 12 weeks or matching placebo. The chances of receiving anamorelin or placebo are 1 in 2. Which subject receives anamorelin or placebo will be decided at random. Neither the subject nor the study doctor will know which study drug the subject is receiving. The subject will be asked to visit the clinic at Day 1, Day 28, Day 56 and Day 84. There will also be a Day 112 follow-up visit and the medical records will be checked after that to see how the subjects are doing.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2011-12-07
• Study First Submitted QC: 2012-01-04
• Study First Posted: 2012-01-09
• Study Start: 2012-06
• Primary Completion: 2016-01
• Study Completion: 2016-03
• Results First Submitted: 2017-01-05
• Results First Submitted QC: 2017-01-05
• Results First Posted: 2017-02-24
• Status Verified: 2018-06
• Last Update Submitted: 2018-06-22
• Last Update Posted: 2018-07-17

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Must have incurable, histologically or cytologically documented Non-Small Cell Lung Cancer or Colo-rectal Cancer.
• Females and males at least 18 years of age.
• Documented histologic or cytologic diagnosis of American Joint Committee on Cancer (AJCC) unresectable Stage III or IV NSCLC and/or stage III or IV colorectal cancer (CRC) (not amenable to curative resection).
• Involuntary weight loss of 5% body weight over a period of 6 months.
• Eastern Cooperative Oncology Group (ECOG) performance status 2 at screening.
• Estimated life expectancy of greater than 4 months at the time of screening.
• Presence and functional use of both hands.
• Able to understand and comply with the procedures of the handgrip strength evaluation.
• If the patient is a woman of childbearing potential or a fertile man, he/she must agree to use an effective form of contraception during the study and for 28 days following the last dose of study medication.
• Willing and able to give signed informed consent and, in the opinion of the Investigator, to comply with the protocol tests and procedures.

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Exclusion Criteria

• Other forms of lung cancer.

• Women who are pregnant or breast-feeding.

• Obesity.

• Recent active excessive alcohol or illicit drug use current use of marijuana or history of marijuana use over the previous 6 months.

• Severe depression.

• Other causes of cachexia such as:

  • Liver disease (AST or ALT > 3x normal levels)
  • Renal failure (creatinine > 2.5 mg/dL)
  • Untreated thyroid disease
  • Class III-IV CHF
  • AIDS
  • Other cancer diagnosed within the past five years other than non-melanoma skin cancer and prostate cancer
  • Severe COPD requiring use of home O2.

• Inability to increase food intake.

• Recent administration of highly emetogenic chemotherapy.

• Known HIV, active hepatitis B or C (with increased LFTs), or active tuberculosis.

• Patients who have received two prior regimens of cytotoxic chemotherapy and are undergoing, or planning to undergo, a third regimen of cytotoxic chemotherapy.

• Currently taking prescription medications intended to increase appetite or treat weight loss; these include, but are not limited to:

  • Testosterone
  • Androgenic compounds
  • Megestrol acetate
  • Methylphenidate
  • Dronabinol

• Current use of steroids or history of use over the previous 6 months except as pre- and post-medications for chemotherapy administration.

• Patients unable to readily swallow oral tablets.

• An active, uncontrolled infection.

• Uncontrolled diabetes mellitus.

• Known or suspected brain metastases.

• Patients receiving strong CYP3A4 inhibitors.

• Patients receiving tube feedings or parenteral nutrition.

• Patients with any concomitant medical or psychiatric condition or social situation that would make it difficult to comply with protocol requirements, including the inability to comply with handgrip strength determinations in both hands; for example, pre-existing neurological impairment.

• Previous exposure to Anamorelin HCl.

• Patients actively receiving a concurrent investigational agent, or any patients that have received an investigational agent within four weeks prior to randomization.

• Current use of diuretics or history of intermittent diuretic usage for any reason over the previous 3 months.

• History of claustrophobia.

• Cachexia deemed by the investigator to be solely due to chemo or radiation treatment

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm 2 (Placebo)	Placebo	Placebo
Arm 1 (Anamorelin HCl)	Anamorelin HCl	Anamorelin HCl

Primary Outcome Measures

Name	Time	Method
Total Body Potassium.	day 84	percentage change from baseline

Secondary Outcome Measures

Name	Time	Method
Functional Performance.	day 84	Functional performance using stair-climbing power day 84 percent change from baseline
Body Composition.	day 84	Body composition as measured by Total body nitrogen. Percentage of change day 84-baseline
Muscle Strength as Measured by Grip Strength.	day 84	Dominant hand grip strength day 84 - percent change from baseline
Body Weight.	day 84	percent change from day 84-baseline
Appetite.	day 84	Appetite measured by a visual analogue scale ASAS. Percentage of change day84-baseline
Stair Climbing Power	day 84	Percent change from baseline
Food Diary Calorie Count	day 84	change between day 84 and baseline
Lean Mass Measured by Densitometry.	day 84	lean body mass measured by DEXA. Percentage of change day 84-baseline.
Resting Energy Expenditure.	day 84	% change between day 84 and baseline
1-repetition Max. Strength	day 84	leg extension - percentage of change day 84 to baseline
Quality of Life.	day 84	Quality of life as assessed using the FACIT-F Patient Reported Outcome assessments - percentage of change day 84-baseline

Trial Locations

Locations (1)

Michael E. DeBakey VA Medical Center, Houston, TX; 🇺🇸 Houston, Texas, United States