CBD in Postmenopausal Women With Osteopenia

Canopy Growth

Status and phase: Terminated; Phase 1

Conditions: Osteopenia

Treatments: Drug: CBD; Other: Placebo

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT05317013

710022US1314

Details and patient eligibility

About

This is a Phase 1, double-blind, placebo-controlled, repeated-dose study to assess the safety, tolerability, and preliminary effects of CHI-554 in postmenopausal women ages 50-80 years who have osteopenia.

Enrollment: 2 patients

Sex: Female

Ages: 50 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Is a female aged 50-80 years, inclusive, at the time of screening.
• Is postmenopausal, defined as > or = 12 months amenorrhoea.
• Has osteopenia, defined as T score at lumbar spine or femoral neck or total femur of less than -1.0, but not less than or equal to -2.5, according to dual energy x-ray absorptiometry (DXA) completed at the Screening Visit or performed at NM Clinical Research & Osteoporosis Center up to 6 months prior to the Screening Visit.
• Has been on a stable dose of 500 mg calcium daily for at least 7 days prior to Visit 1.
• Has a body mass index between 18 and 35 kg/m2 (inclusive).
• Is judged by the Investigator to be in generally good health at screening based on participants' medical history.
• Must be adequately informed of the nature and risks of the study and give written informed consent prior to screening.

Exclusion criteria

• Has a history of epilepsy, hepatitis, or human immunodeficiency virus.
• Current or history of use of one or more prohibited medications (as described in Section 8.2.1.1).
• Changes in the use of a prescription, over-the-counter (OTC), systemic or topical drug(s), herbal supplement(s), or vitamin(s) for the 4 weeks prior to the Screening Visit.
• Evidence of clinically significant hepatic or renal impairment including alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >1.5× the upper limit of normal (ULN), or bilirubin >2× ULN.
• Has any clinically significant condition or abnormal finding at screening that would, in the opinion of the Investigator, preclude study participation or interfere with the evaluation of the study IP.
• Has a history of a known significant allergic condition, significant drug-related hypersensitivity, or allergic reaction to any compound or chemical class related to cannabis, including phytocannabinoids and cannabinoid analogues, or excipients utilized within the IP (e.g., coconut; coconut oil; medium-chain triglycerides).
• Has taken grapefruit products and/or Seville oranges within the 7 days prior to Visit 1.
• Positive urine dipstick results for THC at the Screening Visit.
• Has a history or current diagnosis of a significant psychiatric disorder, including alcohol or substance use disorder, that would, in the opinion of the Investigator, affect the subject's ability to comply with the study requirements.
• Has participated in any investigational product or device study within 30 days prior to the Screening Visit, or is scheduled to participate in another investigational product or device study during the course of this study.
• Demonstrates behavior indicating unreliability or inability to comply with the requirements of the protocol.
• History of Osteoporosis diagnosis.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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2 participants in 3 patient groups, including a placebo group

Group A - 100 mg CBD

Experimental group

Description:

100 mg CBD per day

Treatment:

Drug: CBD

Group B - 300 mg CBD

Experimental group

Description:

300 mg CBD per day

Treatment:

Drug: CBD

Group C - Placebo

Placebo Comparator group

Description:

Placebo

Treatment:

Other: Placebo