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BHB & CAR-T for Lymphomas

NCT06610344 · Abramson Cancer Center at Penn Medicine
In plain English

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Official title
Preliminary Investigation of β-hydroxybutyrate Supplementation for Lymphoma Patients Receiving Anti-CD19 CAR T-cells
About this study
The aim of this study is to assess the feasibility of β-hydroxybutyrate (BHB) supplementation in individuals who are receiving therapy for lymphoma with standard-of-care anti-CD19 CAR T-cells (CAR-T) to determine whether BHB supplementation is safe and tolerable in this patient population. Additionally, this study will determine whether BHB supplementation leads to changes the gut microbiome and peripheral blood mononuclear cells (PBMCs). BHB supplementation will be performed through oral administration of HVMN Ketone-IQ, a commercially available BHB supplement, with an active ingredient of R- 1,3-Butanediol, which is converted to BHB.
Eligibility criteria
Inclusion Criteria: * Age of 18 years or older * History of pathologically-confirmed large B-cell lymphoma (LBCL) * Planned treatment with a commercially available anti-CD19 CAR-T product (Yescarta or Kymriah) * Eligible for and with adequate organ function (investigator discretion) and performance status (ECOG PS 2 or less) for standard of care, anti-CD19 CAR-T * Not enrolled on a clinical trial of bridging therapy prior to CAR-T * Patients must have a PET/CT scan (preferred), diagnostic CT scan, or MRI with at least one bi-dimensionally measurable lesion (≥ 1.5 cm for nodal lesions or ≥ 1cm for extra- nodal lesions in largest dimension by low-dose computerized tomography \[CT\] scan with FDG-uptake ≥ liver) documented prior to leukapheresis for CAR-T manufacturing * Resolution of toxicities from prior therapy to a grade that does not contraindicate trial participation in the opinion of the investigator * Can provide informed consent * Willing to comply with all study procedures and available for the duration of the study Exclusion Criteria: * Subject is pregnant or breast feeding * History of allergy to energy drinks * History of inflammatory bowel disease * History of type 1 diabetes mellitus or requirement for insulin * History of chronic kidney disease with an eGFR \< 30 mL/min/1.73m2 * Additional second primary malignancy for which the subject is receiving active therapy or that will impede the ability of the investigator to assess lymphoma response
Study design
Enrollment target: 5 participants
Allocation: na
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2025-01-07
Estimated completion: 2027-09-15
Last updated: 2026-02-23
Interventions
Dietary Supplement: R-1,3-Butanediol
Primary outcomes
  • Safety and tolerability (From CART infusion to day 28 visit after CART)
Sponsor
Abramson Cancer Center at Penn Medicine · other
Contacts & investigators
ContactBrittany Koch, MPH · contact · Brittany.Koch@pennmedicine.upenn.edu · 215-615-4312
ContactKaitlin Kennard, BSN, RN · contact · Kaitlin.Kennard@pennmedicine.upenn.edu · 267-804-4080
InvestigatorElise Chong, MD · principal_investigator, Abramson Cancer Center at the University of Pennsylvania
All locations (1)
Abramson Cancer Center at University of PennsylvaniaRecruiting
Philadelphia, Pennsylvania, United States
BHB & CAR-T for Lymphomas · TrialPath