Oral 5 Strain Probiotic for GI Toxicity Mitigation During Pelvic Radiation

Not Applicable

Not yet recruiting

• Conditions: Radiation Injuries
• Interventions: Biological: Pendulum Glucose Control (PGC)

• Registration Number: NCT07231588
• Lead Sponsor: University of Cincinnati

Brief Summary

This research is to determine if an oral probiotic, Pendulum Glucose Control (PGC), can be safely given to patients during pelvic radiation therapy (RT). The researchers will study if the probiotics lessen gastrointestinal toxicity during pelvic radiation.

Detailed Description

The exact mechanism of GI symptoms is elusive, but there is sufficient data to suggest that the intestinal microbiome plays a role in radiation-induced GI injury. The investigators propose a pilot feasibility trial evaluating whether an oral 5 strain probiotic (PGC) can be safely and effectively administered during pelvic RT. PGC will be supplied by Pendulum Therapeutics. Pendulum has completed trials using PGC in non-cancer conditions \[26\]. The investigators hypothesize that oral supplementation with PGC for GI toxicity mitigation during pelvic radiation is feasible. The intervention will be considered feasible if probiotic tolerability and patient adherence are appropriate. An overall probiotic adherence rate of ≥ 80% by ≥ 70% of patients will be considered acceptable. If feasible, these results will support evaluation of toxicity mitigation in randomized subsequent Phase II/III trials of PGC supplementation during pelvic radiation.

Study Timeline

• Status Verified: 2025-11
• Study First Submitted: 2025-11-12
• Study First Submitted QC: 2025-11-14
• Last Update Submitted: 2025-11-14
• Study First Posted: 2025-11-17
• Last Update Posted: 2025-11-17
• Study Start: 2025-12-01
• Primary Completion: 2026-06-01
• Study Completion: 2026-12-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Patients must have histologically confirmed malignancy for which the standard of care treatment is at least 30 Gy of pelvic RT to the pelvic lymph nodes.

   a. Eligible diagnoses include: i. Lower GI cancers (anal, rectal) ii. Gynecologic cancers (cervical, vulvar, vaginal, endometrial) iii. Prostate cancer with lymph node involvement

2. Age ≥18 years.

3. ECOG performance status ≤2 (or Karnofsky ≥60%, see Appendix A).

4. Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

1. Patients with inflammatory bowel disease (IBD - such as Crohn's or Ulcerative Colitis).

2. Patients who are currently receiving any other investigational agents. Patients who have received other investigational agents previously who are no longer receiving these investigational agents may be eligible at the discretion of the PI.

3. Patients with uncontrolled intercurrent illness or any other significant condition(s) that would make participation in this protocol unreasonably hazardous, in the opinion of the Investigator.

4. Patients with a prior or concurrent malignancy whose natural history or treatment have the potential to interfere with the safety or efficacy assessment of the investigational regimen in the opinion of the Investigator.

5. Patients who have received previous radiation therapy to the pelvis at any time.

6. Patients who have not recovered from GI adverse events due to previous cancer therapy.

7. Patients with colostomy or ileostomy.

8. Pregnant women are excluded from this study because they cannot receive radiotherapy.

9. Known inulin intolerance or allergies or hypersensitivity to any of the components of PGC, including:

   1. Known hypersensitivity to >4 first-line antimicrobial therapies against Akkermansia muciniphila, Clostridium beijerinckii, Clostridium butyricum, Anaerobutyricum hallii: Penicillin, Piperacillin, Tetracycline, Amoxicillin, Ampicillin
   2. Known hypersensitivity to >4 first-line antimicrobial therapies against Bifidobacterium infantis Bi-26TM: Gentamicin, Kanamycin, Streptomycin, Tetracycline, Erythromycin, Clindamycin, Ampicillin, Vancomycin

10. Patients unable to swallow capsules.

11. Absolute Neutrophil Count (ANC) < 1500/uL.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
RT + Probiotic	Pendulum Glucose Control (PGC)	Pendulum Glucose Control (PGC) probiotic + Radiation Therapy Treatment

Primary Outcome Measures

Name	Time	Method
Pendulum Glucose Control (PGC) Probiotic Adherence Rate (PAR)- measured by pill counts	Week 6 and week 10	1\. To evaluate Pendulum Glucose Control (PGC) Probiotic Adherence Rate (PAR).; a. To assess Probiotic Adherence Rate (PAR), pill counts will be conducted at week 6 and week 10.

Secondary Outcome Measures

Name	Time	Method
Physician-reported GI toxicity with the addition of PGC - measured by CTCAE v6	Baseline, week 4, week 6 and week 10. Week 14 (safety visit)	To assess physician-reported GI toxicity, AEs using CTCAE v6 will be collected at baseline, week 4, week 6 and week 10. This will also be assessed at the 30 day safety visit after patients discontinue the supplement.
Patient-reported GI toxicity with the addition of PGC measured by PRO-CTCAE	Baseline, week 4, week 6 and week 10. Week 14 (safety visit)	To assess patient-reported GI toxicity, an EPIC Bowel and a customized PRO-CTCAE will be collected at baseline, week 4, week 6 and week 10. This will also be assessed at the 30 day safety visit after patients discontinue the supplement.

Trial Locations

Locations (1)

University of Cincinnati Medical Center; 🇺🇸 Cincinnati, Ohio, United States