Safety, Tolerability, and Pharmacodynamics of SYNB8802v1 in Subjects With History of Gastric Bypass Surgery or Short-bowel Syndrome

Synlogic

Status and phase

Completed

Early Phase 1

Conditions

Enteric Hyperoxaluria

Treatments

Other: Placebo

Drug: SYNB8802v1

Study type

Interventional

Funder types

Industry

Identifiers

NCT05377112

SYNB8802-CP-002

Details and patient eligibility

About

Study SYNB8802-CP-002 is designed to assess safety, tolerability, and oxalate lowering, in subjects with a history of gastric bypass surgery or short-bowel syndrome. In addition, this study will explore other PD effects relative to baseline as well as predictors of efficacy and tolerability.

Full description

This is a double-blind (sponsor-open), randomized (3:2), placebo-controlled, inpatient study evaluating the safety and tolerability of SYNB8802v1 in subjects with a history of gastric bypass surgery or short-bowel syndrome. An interim analysis of results by an unblinded statistician will be performed after 10 subjects.

The study includes the following periods:

Screening period (27 days)
Diet run in (3 days)
Dosing Period (12 days)
Safety follow-up (28 days)

The maximum duration of the inpatient stay will be 17 days (Day -4 to Day 13). Subjects will report to the clinical research unit (CRU) on Day -4 and will complete a 3-day diet run-in period (Days -3 to -1) during which they will consume an AOLC diet (refer to Diet Manual for details). Dietary oxalate and calcium will be distributed across 3 meals per day, and subjects will maintain this diet until the end of the dosing period. A proton pump inhibitor (PPI, esomeprazole) will be administered once daily (QD), 60-90 minutes before breakfast, from the start of the diet run-in period (Day -3) until the end of the dosing period (Day 12).

On Day 1, subjects will be randomly assigned to treatment with SYNB8802v1 or placebo (collectively referred to as investigational medicinal product [IMP]). The dosing period consists of 12 days following a dose escalation plan from 1 × 1011 live cells QD to 3 × 1011 live cells TID; the dosing period for each dose level includes a 2-day dose ramp and a 3-day steady-state period. During the dose ramp, placebo will be administered such that all subjects receive IMP dosing TID. On the morning of the first day of the run-in period (Day -3), a forced void urine sample will be collected to completely empty the bladder before the first placebo dose administration. A 24-hour urine collection will then be started and will continue throughout the in-patient period. In addition, daily 24-hour fecal samples will be collected. Subjects will be released from the CRU upon the completion of safety assessments on Day 13 (the day after the last dose of IMP). Safety follow-up visits (calls) will occur every 7 (±2) days until 28 (±2) days after the last dose of IMP.

Enrollment

11 patients

Sex

All

Ages

18 to 74 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 18 to ≤ 74 years.
Able and willing to voluntarily complete the informed consent process.
Available for, and agree to, all study procedures, including fixed diet, feces, urine, and blood
collection, follow-up visits, and compliance with all study procedures.
History of gastric bypass surgery (at least 12 months prior to Day 1) or short-bowel
syndrome.
If taking probiotic supplements (enriched foods excluded), has been on a stable, well tolerated dose for at least 2 weeks prior to Day 1.
Women of childbearing potential must have a negative pregnancy test (human chorionic
gonadotropin) at screening and at baseline prior to the start of IMP.
Screening laboratory evaluations (e.g., chemistry panel, complete blood count with
differential, prothrombin time, urinalysis) and electrocardiogram (ECG) must be within
normal limits or judged not to be clinically significant by the investigator. Subjects with
known diabetes should be well controlled and have an A1c of ≤ 8% within 3 months prior to Day 1.
Agree to abstain from tobacco/nicotine use for the duration of the inpatient stay.
Subjects who are HIV positive, on therapy with normal CD4 counts and undetectable viral loads, can be included.

Exclusion criteria

Acute or chronic medical (including COVID-19 infection), surgical, psychiatric, or social condition or laboratory abnormality (except those that can be explained by malabsorption) that may increase subject risk associated with study participation, compromise adherence to study procedures and requirements, or may confound interpretation of results and, in the judgment of the investigator, would make the subject inappropriate for enrollment.
Estimated glomerular filtration rate < 45 mL/min/1.73 m2.
History of kidney stones.
Subjects taking supplements that contain vitamin C should continue to use their supplements at a constant dose throughout the study, having maintained a constant dose for 2 weeks prior to screening.
Known primary hyperoxaluria.
Pregnant or lactating.
Administration or ingestion of any type of systemic (e.g., oral or intravenous) antibiotic within 5 half-lives of the agent prior to Day 1. Exception: topical antibiotics are allowed.
Any co-morbid condition that may necessitate antibiotic use or disrupt the controlled diet during the study period.
Intolerance of, or allergic reaction to, EcN, all PPIs, or any of the ingredients in SYNB8802v1 or placebo formulations.
Dependence on alcohol or drugs of abuse.
Current, immunodeficiency disorder including autoimmune, except for controlled HIV (see inclusion Criterion #9). disorders.
Administration or ingestion of an investigational drug within 30 days or 5 half-lives, whichever is longer, prior to screening visit, or current enrollment in an investigational study.
History of inflammatory bowel disease.