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REZIPAS (AMINOSALICYLIC ACID RESIN COMPLEX)

BRISTOL MYERS SQUIBB · FDA-approved approved Under review Quality 20/100

REZIPAS (generic name: AMINOSALICYLIC ACID RESIN COMPLEX) is a drug developed by BRISTOL MYERS SQUIBB. It is currently FDA-approved for Acute tuberculosis, Pulmonary tuberculosis.

REZIPAS, also known as 4-Aminosalicylic acid, is a small molecule dihydrofolate reductase inhibitor. It has been studied in clinical trials for various conditions, including Ulcerative Colitis, HIV Infections, and Sexually Transmitted Diseases, often in comparison to Budesonide MMX or Placebo.

At a glance

Generic nameAMINOSALICYLIC ACID RESIN COMPLEX
SponsorBRISTOL MYERS SQUIBB
TargetTyrosine-protein phosphatase non-receptor type 1, Cyclooxygenase, 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
Therapeutic areaInfectious Disease
PhaseFDA-approved

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about REZIPAS

What is REZIPAS?

REZIPAS (AMINOSALICYLIC ACID RESIN COMPLEX) is a pharmaceutical drug developed by BRISTOL MYERS SQUIBB, indicated for Acute tuberculosis, Pulmonary tuberculosis.

What is REZIPAS used for?

REZIPAS is indicated for Acute tuberculosis, Pulmonary tuberculosis.

Who makes REZIPAS?

REZIPAS is developed and marketed by BRISTOL MYERS SQUIBB (see full BRISTOL MYERS SQUIBB pipeline at /company/bristol-myers-squibb).

What is the generic name of REZIPAS?

AMINOSALICYLIC ACID RESIN COMPLEX is the generic (nonproprietary) name of REZIPAS.

What development phase is REZIPAS in?

REZIPAS is FDA-approved (marketed).

What does REZIPAS target?

REZIPAS targets Tyrosine-protein phosphatase non-receptor type 1, Cyclooxygenase, 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing