Overview

Efficacy and Safety of Dronabinol in the Improvement of Chemotherapy-induced and Tumor-related Symptoms in Advanced Pancreatic Cancer

Status:
Recruiting
Trial end date:
2023-09-30
Target enrollment:
0
Participant gender:
All
Summary
Aim of this phase III trial is to investigate the efficacy and safety of dronabinol (orally administered tetrahydrocannabinol (THC)) as adjuvant therapy to first-line standard chemotherapy in patients with metastatic pancreatic cancer for improvement of chemotherapy- and tumor-related symptoms applicated by individual titration up to the maximum tolerated dose.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Arbeitsgemeinschaft medikamentoese Tumortherapie
Collaborators:
Bionorica SE
Medical University of Graz
Unidata Geodesign
Treatments:
Dronabinol
Criteria
Inclusion Criteria:

- Male and female subjects aged ≥18

- Patients with diagnosis of locally advanced, inoperable or metastatic pancreatic
cancer, eligible for first-line chemotherapy with FOLFIRINOX or gemcitabine+Abraxane®

- According to investigator life expectancy of > 4 months at screening

- Female patients must either be post-menopausal or surgically sterilized or use a
highly effective method of birth control (hormonal contraceptives, intra-uterine
devices, or diaphragms with spermicide) for the duration of the study and/or must have
a negative pregnancy test (female patients with childbearing potential only)

- Willing and able to provide written informed consent.

- Written informed consent given prior to any trial-related procedure not part of the
normal medical practice.

Exclusion Criteria:

- Patients who are members of the staff of the trial center, staff of the sponsor or
CRO, the investigator him/herself or close relatives of the investigator.

- Simultaneous participation in another interventional clinical trial, participation in
another trial with less than 30 days or five half-lives of the IMP (whatever is
longer) to screening, or previous participation in this trial.

- Ineligible for chemotherapy treatment with FOLFIRINOX or gemcitabine+Abraxane®

- Use of dronabinol or cannabis-based medicine with THC as constituent within 6 months
before screening. A urine drug test will be performed during screening phase.

- Use of marihuana within the last 4 weeks and unwillingness to abstain for the duration
of the study. A urine drug test will be performed during screening phase.

- Currently receiving chemotherapy or anticipated use of chemotherapy due to any
condition not related to locally advanced or metastatic pancreatic cancer

- History of or existing cardiac diseases or pathological findings (e.g. chronic
insufficiency NYHA III/IV, severe arrhythmia, unstable angina pectoris, myocardial
infarction within the past 6 months, significant QT-prolongation etc.), which in the
opinion of the investigator might interfere with the safety or tolerability of the
study treatment. An ECG has to be done to exclude pathological findings and must not
be older than 3 months before screening or if none is available, has to be performed
during the screening phase and assessed prior to randomization

- Clinically relevant, severe pulmonary diseases, uncontrolled hypertension, or poorly
controlled diabetes

- History of or existing relevant CNS and/or psychiatric disorders (e.g. schizophrenia,
psychosis, manic and/or depressive disorders, suicidal ideations, etc) which might
interfere with the safety or tolerability of the study treatment. Patients with
reactive depression are not excluded from participation.

- Known current or past (within the last year prior to screening) alcohol, narcotics or
drug abuse

- Pregnancy or breast feeding

- Known allergy to cannabinoids and other constituents of the investigational medicinal
product

- Intake of prohibited concomitant medication

- Any other substantial medical condition that in the opinion of the investigator could
create undue risk to the subject or could affect adherence with the trial protocol

- Legal incapacity, limited legal capacity or any other condition which makes the
subject unable to understand the subject information and informed consent form (ICF)

- Patients unable or unwilling to waive driving motor vehicles or using machines
especially during titration period

- Unable or unwilling to comply with the protocol regulations