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OncoMatch/Clinical Trials/NCT07167446

Neuroprotective Potential of Cannabidiol (CBD) in Preventing Oxaliplatin (Ox)-Induced Neuropathy

Is NCT07167446 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies multiple treatments including Cannabidiol (CBD) and oxaliplatin-based chemotherapy for oxaliplatin induced peripheral neuropathy in cancer patients.

Early Phase 1RecruitingFox Chase Cancer CenterNCT07167446Data as of May 2026

Treatment: Cannabidiol (CBD) · oxaliplatin-based chemotherapyThis is a pilot, prospective, randomized study evaluating the feasibility and acceptability of incorporating hemp-derived cannabidiol (CBD) supplementation to prevent oxaliplatin-induced peripheral neuropathy (OIPN) in patients receiving oxaliplatin-based chemotherapy for colorectal cancer (CRC). Participants will be randomized to receive either CBD capsules in addition to standard therapy or standard therapy alone.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Disease stage

Metastatic disease required

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: platinum-based chemotherapy (oxaliplatin) — metastatic

planned to receive Ox based chemotherapy in metastatic setting (at least 3 months planned). Subjects are allowed to have one cycle of Ox based chemotherapy before enrollment.

Cannot have received: platinum-based chemotherapy

Exception: Subjects are allowed to have one cycle of Ox based chemotherapy before enrollment.

No prior platinum exposure

Lab requirements

Blood counts

appropriate for systemic therapy, as per physician's discretion

Kidney function

appropriate for systemic therapy, as per physician's discretion

Liver function

Total Bilirubin: <= 1.5 X ULN; AST(SGOT)/ALT(SGPT): <= 3 X ULN (5 X ULN in patients with liver metastases)

Patients must have marrow and organ function appropriate for systemic therapy, as per physician's discretion, but liver function should meet criteria below: Total Bilirubin: less than and/or equal to 1.5 X ULN; AST(SGOT)/ALT(SGPT): less than and/or equal to 3 X ULN (5 X ULN in patients with liver metastases)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Fox Chase Cancer Center · Philadelphia, Pennsylvania

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