Evaluation of TRC101 in Subjects With Metabolic Acidosis Associated With Chronic Kidney Disease

Tricida

Status and phase: Completed; Phase 3

Conditions: Metabolic Acidosis

Treatments: Drug: TRC101; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT03317444

2016-003825-41 (EudraCT Number)

TRCA-301

Details and patient eligibility

About

This is a multicenter, double-blind, placebo-controlled, parallel-design study. The study will enroll approximately 210 adult male and female subjects with stage 3 or 4 chronic kidney disease and metabolic acidosis. The study dosing (TRC101 or placebo) will continue for 12 weeks once daily.

The maximum study duration is anticipated to be up to 16 weeks.

Enrollment: 217 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

• Blood bicarbonate level of 12 to 20 mEq/L.
• Estimated glomerular filtration rate (eGFR) of 20 to 40 mL/min/1.73m2.
• Stable kidney function defined as <=20% variability in eGFR during screening period.

Key Exclusion Criteria:

• Any level of low blood bicarbonate during the screening period that in the opinion of the Investigator, requires emergency intervention or evaluation for an acute acidotic process.
• Anuria, dialysis, acute kidney injury, or history of acute kidney insufficiency within 3 months prior to screening.
• Heart failure with maximum New York Heart Association (NYHA) Class IV symptoms or that required hospitalization during the preceding 6 months.
• Heart or kidney transplant.
• Chronic obstructive pulmonary disease (COPD) that is treated with chronic oral steroids, that requires the subject to be on oxygen, or that required hospitalization within the previous 6 months.
• Change in doses to alkali therapy in the 4 weeks prior to screening.
• History or current diagnosis of diabetic gastroparesis, bowel obstruction, swallowing disorders, inflammatory bowel disease, major gastrointestinal surgery, frequent diarrhea or active gastric/duodenal ulcers.
• Serum calcium <= 8.0 mg/dL at screening.
• Planned initiation of renal replacement therapy within 12 weeks following randomization.
• Use of polymeric binder drugs within 14 days prior to screening.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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217 participants in 2 patient groups, including a placebo group

TRC101

Experimental group

Description:

Administered once daily (QD) for 12 weeks

Treatment:

Drug: TRC101

Placebo

Placebo Comparator group

Description:

Administered once daily (QD) for 12 weeks

Treatment:

Drug: Placebo