Trial Details

Life's End Benefits of cannaBidiol and tetrahYdrocannabinol (LiBBY)

NCT05644262

RECRUITING

DESCRIPTION

This is a multicenter randomized double-blind placebo-controlled Phase 2 study of an oral combination of tetrahydrocannabinol (THC) and cannabidiol (CBD) compared to placebo over 12 weeks. This study is designed to test the hypothesis that treatment with an oral combination of THC/CBD will reduce agitation hospice care-eligible patients with agitation and dementia as measured by the Cohen Mansfield Agitation Inventory (CMAI) when compared to placebo at 2 weeks. This study will enroll approximately 120 participants of any gender at least 40 years of age who are hospice care-eligible with agitation and dementia (HAD). Participants will be randomized (50:50) to either active study drug (T2:C100) or placebo. The double-blind period of this study is 12 weeks. A 12 week optional open-label extension will be offered to participants who complete the double-blind period.

CONDITIONS

ELIGIBILITY CRITERIA

• Inclusion Criteria
• : 1. Provision of signed and dated informed consent from participant or legally authorized representative. 2. Person of any sex/gender 40 years of age or older. 3. Ability to take or be administered liquid medication. 4. Meets DSM-V criteria for Major Neurocognitive Disorder. 5. Current clinically significant agitation as demonstrated by an NPI-agitation subscale of 4 or above at Screening. 6. Meets at least one of the following requirements: 1. Currently enrolled in out-patient or in-patient hospice care. 2. Stage 6d on the Functional Assessment Staging Test (FAST). 3. Score of 12 or more according to the Advanced Dementia Prognostic Tool (ADEPT) as implemented by the Mitchell Index. 7. Willing to agree not to use cannabinoids in any form (e.g., topically applied, ingested, inhaled, or other form of administration), other than the trial medication, during the first 12 weeks of the study. 8. Has a third-party clinician (e.g., hospice, palliative care, PCP) who is responsible for medical management of the participant outside the study. 9. In the opinion of the investigator, resides in an environment suitable to conduct a clinical trial (i.e., study intervention can be administered and concomitant medication use can be accurately documented). 10. In the opinion of the site PI, has a study partner (may be paid or unpaid caregiver) able and willing to provide accurate information about the participant, oversee the administration of study drug, and participate in study visits and informant-based assessments (usually requires at least 5 hours of contact per week). NOTE: Other knowledgeable informants/informed caregivers may contribute to informant-based scales; however, the site should identify an informant who will be able to serve as the primary source of information. 11. As assessed by investigator, participant is likely to be able to comply with the protocol for a minimum of 2 weeks.