Recruiting
Early Phase 1

CBD

Sponsor:

Fox Chase Cancer Center

Code:

NCT07167446

Conditions

Oxaliplatin Induced Peripheral Neuropathy in Cancer Patients

Metastatic Colorectal Cancer (CRC)

Peripheral Neuropathy Due to Chemotherapy

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Cannabidiol (CBD)

oxaliplatin-based chemotherapy

Study Details

Brief summary:

This 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.

Conditions

Oxaliplatin Induced Peripheral Neuropathy in Cancer Patients

Metastatic Colorectal Cancer (CRC)

Peripheral Neuropathy Due to Chemotherapy

Study ID

NCT07167446

Start date

Oct 14, 2025

Status verified date

Oct, 2025

Completion date

Sep 7, 2028

Anticipated

Primary completion date

Sep 5, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Patients with metastatic, locally advanced unresectable colorectal cancer patients planned to receive Ox based chemotherapy in metastatic setting (at least 3 months planned).
2. Subjects are allowed to have one cycle of Ox based chemotherapy before enrollment.
3. ECOG PS 0-2
4. No prior platinum exposure
5. No evidence of ongoing neuropathy of any grade at the time of enrollment
6. Patients must have marrow and organ function appropriate for systemic therapy, as per physician's discretion, but liver function should meet criteria below:

1. Total Bilirubin: less than and/or equal to 1.5 X ULN
2. AST(SGOT)/ALT(SGPT): less than and/or equal to 3 X ULN (5 X ULN in patients with liver metastases
7. Ability to understand and willingness to sign a written informed consent and HIPAA consent document.

Exclusion Criteria:
8. Family history of genetic/familial neuropathy and personal history of ongoing neuropathy (any grade) or nervous system disease with the potential to affect cognition, Parkinson's disease, or multiple sclerosis.
9. Routine use of recreational marijuana products (defined as > 4 times per month) or illicit drug use per self-reported history within the last 90 days. If using medical cannabis products, it should be stopped at least 1 week prior to inclusion.
10. Known underlying liver disease (Child-Pugh B or C) or baseline elevation of total bilirubin greater than and/or equal to 1.5 x upper limit of normal based on screening laboratory values.
11. 1Untreated brain metastases (can increase seizure risk), or treated brain metastases on anti-seizure medications.
12. Patients being treated with anti-seizure or anti-psychotic medications. Patients with a prior history of anti-seizure medication use, who have been off treatment for more than 3 months, are eligible. Use of Selective Serotonin Reuptake Inhibitors (SSRIs) is permitted.
13. Concomitant treatment with strong inducers of CYP3A4 and/or strong inducers of CYP2C19.
14. Underlying history of epilepsy/recurrent seizure disorder or unexplained seizure within past 6 months.
15. Patients with current or lifetime diagnosis of schizophrenia spectrum disorder, psychotic disorder, bipolar disorder type I \& II, cluster B personality disorders (antisocial, borderline, narcissistic, histrionic), eating disorders, as defined by Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revised (DSM-5-TR, APA 2022)
16. Recent history or clinical concern for major depression with suicidal ideation as determined by investigator assessment at baseline
17. Currently taking medications known to be contraindicated with Epidiolex -FDA-approved CBD (buprenorphine, leflunomide, levomethadyl acetate, lomitapide, mipomersen, pexidartinib, propoxyphene, sodium oxybate, teriflunomide, clobazam, lamotrigine, valproate).
18. Women who are pregnant or breastfeeding, and individuals of any sex who are capable of reproduction and unwilling to use an effective form of birth control (e.g., condoms, diaphragm, birth control pills, or IUD).
19. Patients may not be receiving any other investigational agents.

Study Design

Enrollment

30 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Cannabidiol (CBD)

Participants receive hemp-derived cannabidiol (CBD) capsules in addition to standard oxaliplatin-based chemotherapy.

active comparator: Standard of Care

Participants receive standard oxaliplatin-based chemotherapy without CBD supplementation

Interventions

Cannabidiol (CBD)

Oral hemp-derived CBD capsules, 150 mg twice daily (with titration in Cycle 1; dose reductions permitted for tolerability). Administered starting the day before oxaliplatin infusion and continued for 7 days after each chemotherapy cycle.

oxaliplatin-based chemotherapy

Standard of care oxaliplatin-based regimens per NCCN guidelines (e.g., FOLFOX or CAPEOX), administered in 2-3 week cycles for a maximum of 6 months.

Primary outcome measure

  • Proportion of participants adherent to the CBD supplementation protocol at Week 12, as determined by pill counts, patient self-report, and clinic compliance logs. [ Time Frame: Baseline through Week 12 of treatment ]
  • Acceptability of CBD supplementation as measured by the Feasibility of Intervention Measure (FIM) [ Time Frame: Baseline through Week 12 of treatment ]

Central Contacts and Locations

Central contacts

Locations

Fox Chase Cancer Center

Recruiting

Philadelphia, Pennsylvania, United States, 19111

Contacts

More Information

Sponsor

Fox Chase Cancer Center

Last update posted

Oct 22, 2025

Last verified

Oct, 2025

Keywords

  • Oxaliplatin-Induced Peripheral Neuropathy (OIPN)
  • Cannabidiol (CBD)
  • Colorectal Cancer (CRC)
  • Neuroprotection

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Fox Chase Cancer Center on 2025-10-22.