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Cancer CachexiaNCT02359123

Cannabics Capsules as Treatment to Improve Cancer Related CACS in Advanced Cancer Patients

A study testing Cannabics capsules in people with Cancer Cachexia and Atypical Anorexia Nervosa, run by Cannabics Pharmaceuticals Inc. at 1 site in Israel.

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

The main purpose in the treatment of patients with advanced cancer and cancer anorexia cachexia syndrome (CACS) is to prolong life and to improve quality of life (QoL) as far as possible. QoL in patients with CACS is directly related to loss of appetite and loss of weight. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer Cachexia, Atypical Anorexia Nervosa
What is being tested?
Cannabics capsules
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
24 participants
Where
1 siteIsrael
Study dates
Nov 2016to 1 Apr 2018
Phase
Interventional
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

  • Age above 18 years
  • Histological evidence of an incurable malignancy
  • Estimated life expectancy ≥3 months
  • Performance status ≤2 (ECOG classification)
  • Self-report of weight loss of at least 3kg during the preceding 2 months and/or a dietitian-estimated caloric intake of less than 20 calories/kg of body weight per day
  • Patient believes that loss of appetite or loss of weight is an ongoing problem for him
  • Use of chemotherapy or radiotherapy is permitted
  • Sign of written informed consent

Who cannot join

  • Ongoing use of tube feedings or parental nutrition
  • Edema or ascites
  • Central nervous system metastases or brain tumors (patients with stable disease in the brain 28 days after treatment can be included in the study)
  • Treatment with adrenal corticosteroids (except for short-term dexamethasone during time of chemotherapy), androgens, progestational agents or other appetite stimulants within the previous two weeks
  • Insulin-requiring diabetes
  • Pregnancy or lactation or unwillingness to use oral contraceptives
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  • Other life-threatening medical conditions
  • Anticipated alcohol or barbiturate use during the study period
  • Mechanical obstruction of the alimentary tract, malabsorption, or intractable vomiting
  • Use of cannabis or synthetic cannabinoids in the last four weeks

Trial locations and contacts

1 site in 1 country.

Israel1 site
  • Rambam MC

    Haifa

Other trials in Israel

About this study

Official title: Cannabics Capsules as Treatment to Improve Cancer Related Cachexia and Anorexia Syndrome in Advanced Cancer Patients- Pilot Study

The main purpose in the treatment of patients with advanced cancer and cancer anorexia cachexia syndrome (CACS) is to prolong life and to improve quality of life (QoL) as far as possible. QoL in patients with CACS is directly related to loss of appetite and loss of weight. Cannabis pills are given in Israel to advanced cancer patients with various symptoms in order to improve their QoL. There is data on safety/toxicity of cannabis, and these pills are given under the regulations of the Israel Ministry of Health.

The purpose of this study is to examine the influence of Cannabics capsules on improving loss of appetite and loss of weight.

Read the detailed description

Cannabis has long been suggested to stimulate appetite, decrease nausea and vomiting, and improve quality of life in cancer patients. Studies on the efficacy of cannabis for improving CACS and S-NIS have had mixed results. After trials showing improvement in weight gain among AIDS patients, cannabinoids were tested on cancer patients as well. In a controlled, random study comparing dronabinol to a placebo among cancer patients, dronabinol was associated with increased appetite in 38% vs 8% for placebo, and decreased nausea in 20% vs 7%, using acceptable measurement scales. Of the dronabinol patients, 22% gained ≥2 kg, compared with 10.5% of placebo recipients, but this datum did not reach significance, perhaps due to the advanced stage of cancer and the high mortality in both placebo and experimental group (30).

Another randomized study compared dronabinol to megestrol acetate or both treatments together. The research included 469 advanced cancer patients who had been suffering from a substantial appetite loss. A greater percentage of megestrol acetate-treated patients reported appetite improvement compared with dronabinol-treated patients, 75% vs 49% (p=0.0001). Combination treatment resulted in no significant differences compared with megestrol acetate alone. Another study, which included 243 patients, compared the administration of a combination of tetrahydrocannabinol and cannabinol to tetrahydrocannabinol alone, compared to placebo. It should be noted that cannabinoid dosages in the study were low, even in comparison to other studies. No significant differences between the groups were seen regarding improvement in appetite or weight-gain. In these two studies, no substantial side effects of cannabis products were found compared to the other arms. This may be related to the dosages of the drugs given.

A more recent study demonstrated improved chemosensory perception, appetite, sleep, and macronutrient preference in advanced cancer patients. However, the study included less than 50 patients. This research showed improvement in taste and smell perception in patients receiving chemotherapy, as well as appetite and caloric intake in the arm that received dronabinol compared to placebo.

Assessment: Base-line assessment

  1. Physician anamnesis and physical examination
  2. Complete blood cell count (CBC) and biochemistry test: electrolytes, renal and liver function tests, albumin level, total cholesterol level
  3. Blood test for TNF-alpha level
  4. Nutrition evaluation, including daily caloric calculation (by using 3 day food diary) and weighting the patient
  5. QoL assessment by EORTC C30 and Anorexia/Cachexia Therapy assessment by FAACT questionnaire
  6. Evaluation of muscle strength by using hand dynamometer as estimation for muscle mass.

Treatment assessment

  1. Physician anamnesis including toxicity assessment according to CTCAE recommendations for acute toxicity, and physical examination including weighing the patient every two weeks in the first month, every month in the coming two months, and every six weeks in the next three months
  2. CBC, biochemistry blood test, TNF-alpha level on day 1, and after three months
  3. Nutritional intake evaluation on the first week and after three months, based on daily caloric calculation of three day food diary
  4. Muscle strength evaluation on day 1 and after three months
  5. QOL assessment by EORTC C30 and Anorexia/Cachexia Therapy assessment by FAACT questionnaire on day 1 and after three and six months
  6. Safety assessment for early psychiatric side-effects by the Community Assessment of Psychic Experiences (CAPE) questionnaire on day 1 and after 2 weeks and after 3 months.
  7. Urine THC- levels one day 1, 2 weeks, 3 months.

Quality-of-Life (QOL) Assessment

QOL will be assessed using the European Organization of Research and Treatment of Cancer core questions on the Quality of Life Questionnaire, version 2 (QLQ-C30) (43) and the Anorexia/Cachexia Therapy (FAACT) questionnaire (44).

Nutrition assessment

  1. Daily caloric calculation will be based on the three day food diary. On day 1, the patient will meet the dietitian and receive guidance and instruction of how to complete the diary. The cannabis pills will be given on day 4, after bringing back the three day diary. After three months, the patient will again do a three day food diary and caloric calculation will be made.
  2. The caloric calculation will be made with the Ministry of Health Computer software "Zameret".
  3. The patient will have telephone support from the dietitian as needed during the days of the diary completion.
  4. Cannabics capsules will be given on day 4, after bringing back the three day diary.

Safety assessment:

Community Assessment of Psychic Experiences (CAPE) questionnaire to evaluated possible early psychiatric side-effects will be given in 3 time points, together with measuring the THC level in the urine. Evaluation of other side-effects will be done in every physician visit.

Being tested
Cannabics capsules

What participants receive

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

  • Cannabics capsulesOther

    Also called Cannabics SR

    Cannabis extract in an oil formulation

Study groups in NCT02359123
Study groupRoleWhat they receive
Cannabics 5mgExperimentalPatients will be treated initially for 3-4 days with 1x5mg Cannabics capsules per day for gradual adaptation. From the 5th day, patients will be treated 2x5mg capsules per 24 hours for a period of 3 months. However, since some patients may suffer from side effects mainly, dizziness and or anxiety, dosage for these patients will be reduced to 5mg per day.
Receives: Other: Cannabics capsules

What is being measured

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

  1. weight gain of ≥10% from baseline weight assessed.

    weight gain of ≥10% from baseline weight assessed by weighing the patient every two weeks in the first month, every month in the coming two months, and every six weeks in the next three months

    Measured: 3 months

Secondary outcomes (7)
  1. Improvement in appetite

    measured by [include analysis, scale, questionnaire, etc.]

    Measured: 3 months

  2. Nutritional intake

    evaluation on the first week and after three months, based on daily caloric calculation of three day food diary.

    Measured: 3 months

  3. Reduction in TNF-alpha

    level assessed by CBC, biochemistry blood test, TNF-alpha level on day 1, and after three months

    Measured: 3 months

  4. Correlation between THC levels and primary outcome,

    assessment by Urine THC- levels one day 1, 2 weeks, 3 months.

    Measured: 3 months

  5. QOL will be assessed using the European Organization of Research and Treatment of Cancer core questions on the Quality of Life Questionnaire, version 2 (QLQ-C30) and the Anorexia/Cachexia Therapy (FAACT) questionnaire.

    will be assessed using the European Organization of Research and Treatment of Cancer core questions on the Quality of Life Questionnaire, version 2 (QLQ-C30) and the Anorexia/Cachexia Therapy (FAACT) questionnaire.

    Measured: 3 months

  6. Safety assessment for early psychiatric side-effects by the Community Assessment of Psychic Experiences

    (CAPE) questionnaire on day 1 and after 2 weeks and after 3 months.

    Measured: 3 months

  7. Evaluation of muscle strength

    using hand dynamometer as estimation for muscle mass on day 1 and after three months.

    Measured: 3 months

Timeline

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

  1. First posted9 Feb 2015 (estimated)
  2. Study startNov 2016
  3. Primary completion1 Apr 2018
  4. Study completion1 Apr 2018

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 N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
24 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02359123
Sponsor's protocol ID
CNBX-001
Status last verified
Apr 2018
First submitted
26 Jan 2015
Last updated
10 Apr 2018
Results posted
No
Data monitoring committee
No

Publications

  • Bar-Sela G, Zalman D, Semenysty V, Ballan E. The Effects of Dosage-Controlled Cannabis Capsules on Cancer-Related Cachexia and Anorexia Syndrome in Advanced Cancer Patients: Pilot Study. Integr Cancer Ther. 2019 Jan-Dec;18:1534735419881498. doi: 10.1177/1534735419881498.

    PubMed 31595793

Questions about this trial

What is this clinical trial studying?

A study testing Cannabics capsules in people with Cancer Cachexia and Atypical Anorexia Nervosa, run by Cannabics Pharmaceuticals Inc. at 1 site in Israel.

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 8 inclusion and 10 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 10 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Israel. 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. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

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?

weight gain of ≥10% from baseline weight assessed. (time frame: 3 months). 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 NCT02359123, 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 10 Apr 2018.

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