Recruiting

β-Hydroxybutyrate

Sponsor:

Abramson Cancer Center at Penn Medicine

Code:

NCT06578637

Conditions

FAP

Familial Adenomatous Polyposis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

R-1,3-Butanediol (10G-A)

R-1,3-Butanediol (20G-A)

R-1,3-Butanediol (30G-A)

R-1,3-Butanediol (30G-B)

Study Details

Brief summary:

The aim of this study is to evaluate the potential of BHB supplementation as a novel strategy to impede the development and progression of intestinal adenomas in individuals with FAP, thus potentially reducing the need for frequent upper endoscopies and colonoscopies and preventing the need for risk-reducing surgical intervention.

Conditions

FAP

Familial Adenomatous Polyposis

Study ID

NCT06578637

Start date

Sep 20, 2024

Status verified date

Aug, 2025

Completion date

Oct, 2027

Anticipated

Primary completion date

Oct, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Part A

Inclusion Criteria:

1. Have a diagnosis of FAP with genetic testing demonstrating a pathogenic or likely pathogenic germline variant in APC, must have a clinical FAP phenotype with at least one member of the family who has a pathogenic or likely pathogenic germline variant in APC, or must have a clinical diagnosis of FAP as agreed by two gastrointestinal cancer genetics experts
2. Must have an extensive colonic resection with either a subtotal colectomy with ileorectal anastomosis (STC-IRA) or total proctocolectomy with ileal pouch anal anastomosis (TPC-IPAA)
3. Can provide informed consent

Exclusion Criteria:

1. Subject is pregnant, a prisoner, or is under 18 years of age
2. Prior total proctocolectomy with end ileostomy
3. History of inflammatory bowel disease
4. History of diabetes mellitus and are currently on medical diabetes therapy
5. History of chronic kidney disease with an eGFR \< 60 mL/min/1.73m2
6. Cancer diagnosis where the subject is receiving active therapy
7. Use of either a ketogenic diet or intermittent fasting (defined as a fasting period of 16 hours or more per day that is not associated with a medical procedure) during the 4 weeks prior to enrollment

Part B

Inclusion Criteria:

1. Have a diagnosis of FAP with genetic testing demonstrating a pathogenic or likely pathogenic germline variant in APC, must have a clinical FAP phenotype with at least one member of the family who has a pathogenic or likely pathogenic germline variant in APC, or must have a clinical diagnosis of FAP as agreed by two gastrointestinal cancer genetics experts.
2. Willing to undergo a colonoscopy or sigmoidoscopy, which may be part of the patient's routine standard care.
3. Able to have a concurrent upper endoscopy performed with the colonoscopy/sigmoidoscopy. This upper endoscopy may be part of the patient's routine standard care.
4. Have at least two colorectal polyps at enrollment (which can be present anywhere in the colon including the rectal cuff, or in the J-pouch \[if applicable\]).
5. Can provide informed consent.

Exclusion Criteria:

1. Subject is pregnant, a prisoner, or is under 18 years of age
2. Patient is not able to undergo colonoscopy/sigmoidoscopy or upper endoscopy
3. Prior total proctocolectomy with end ileostomy
4. History of inflammatory bowel disease
5. History of diabetes mellitus and are currently on medical diabetes therapy
6. History of chronic kidney disease with an eGFR < 60 mL/min/1.73m2
7. Cancer diagnosis where the subject is receiving active therapy
8. Use of either a ketogenic diet or intermittent fasting (defined as a fasting period of 16 hours or more per day that is not associated with a medical procedure) during the 4 weeks prior to enrollment
9. Regular use of any FAP-related chemopreventive agent in the 6 weeks prior to enrollment including aspirin (> 81mg daily), NSAIDs, BHB supplementation, or any other medication deemed a chemopreventive agent by the study investigators
10. Any colonic or small intestinal polyp observed endoscopically that is > 1 cm in size and is not removed (excluding ampullary adenomas)

Study Design

Enrollment

20 participants

Anticipated

Allocation

Non randomized

Intervention Model

Single group

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: Part A - 10 grams

Study participants will take one 35mL dose of HVMN Ketone-IQ by mouth per day (10 total grams of R-1,3-Butanediol) for 2 weeks

experimental: Part A - 20 grams

Study participants will take two 35mL dose of HVMN Ketone-IQ by mouth per day (20 total grams of R-1,3-Butanediol) for 2 weeks

experimental: Part A - 30 grams

Study participants will take three 35mL dose of HVMN Ketone-IQ by mouth per day (30 total grams of R-1,3-Butanediol) for 2 weeks

experimental: Part B - 30 grams

Study participants will take one 35mL dose of HVMN Ketone-IQ by mouth three times per day (30 total grams of R-1,3-Butanediol) for 12 weeks, with a possible additional 12 week extension

Interventions

R-1,3-Butanediol (10G-A)

Study participants will take one 35mL dose of HVMN Ketone-IQ by mouth per day (10 total grams of R-1,3-Butanediol) for 2 weeks

R-1,3-Butanediol (20G-A)

Study participants will take two 35mL dose of HVMN Ketone-IQ by mouth per day (20 total grams of R-1,3-Butanediol) for 2 weeks

R-1,3-Butanediol (30G-A)

Study participants will take three 35mL dose of HVMN Ketone-IQ by mouth per day (30 total grams of R-1,3-Butanediol) for 2 weeks

R-1,3-Butanediol (30G-B)

Study participants will take one 35mL dose of HVMN Ketone-IQ by mouth three times per day (30 total grams of R-1,3-Butanediol) for 12 weeks, with a possible additional 12 week extension

Primary outcome measure

  • Determine whether oral BHB supplementation is safe and tolerable in FAP [ Time Frame: Through study completion, which will be approximately 3 years ]

Central Contacts and Locations

Central contacts

Locations

Abramson Cancer Center of the University of Pennsylvania

Recruiting

Philadelphia, Pennsylvania, United States, 19104

Contacts

Principal Investigator:

Bryson W Katona, MD, PhD

More Information

Sponsor

Abramson Cancer Center at Penn Medicine

Last update posted

Sep 4, 2025

Last verified

Aug, 2025

Keywords

  • FAP
  • Familial adenomatous polyposis
  • Chemoprevention
  • Polyps
  • BHB
  • Beta-hydroxybutyrate

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Abramson Cancer Center at Penn Medicine on 2025-09-04.