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Immediate release torsemide

Sarfez Pharmaceuticals, Inc. · Phase 2 active Small molecule Under review Quality 0/100

Immediate release torsemide is a Loop diuretic Small molecule drug developed by Sarfez Pharmaceuticals, Inc.. It is currently in Phase 2 development for Edema, Hypertension.

Inhibits the sodium-chloride cotransporter in the distal convoluted tubule of the kidneys.

Immediate release torsemide is a small molecule that inhibits the sodium-(potassium)-chloride cotransporter 2, which is a target of the solute carrier family 12 member 1. It is used to treat conditions such as congestive heart failure, chronic kidney diseases, hypertension, heart failure, and edema, as indicated by ClinicalTrials.gov.

Likelihood of approval
13.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Cardiovascular Phase 3 risk -2.0pp
    Modern cardiovascular outcome trials are large + long; many fail to beat aggressive standard-of-care.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameImmediate release torsemide
SponsorSarfez Pharmaceuticals, Inc.
Drug classLoop diuretic
TargetNa-K-2Cl cotransporter 2 (NKCC2)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 2

Mechanism of action

This leads to increased sodium and water excretion, resulting in a diuretic effect.

Approved indications

Common side effects

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

Competitive intelligence

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Frequently asked questions about Immediate release torsemide

What is Immediate release torsemide?

Immediate release torsemide is a Loop diuretic drug developed by Sarfez Pharmaceuticals, Inc., indicated for Edema, Hypertension.

How does Immediate release torsemide work?

Inhibits the sodium-chloride cotransporter in the distal convoluted tubule of the kidneys.

What is Immediate release torsemide used for?

Immediate release torsemide is indicated for Edema, Hypertension.

Who makes Immediate release torsemide?

Immediate release torsemide is developed by Sarfez Pharmaceuticals, Inc. (see full Sarfez Pharmaceuticals, Inc. pipeline at /company/sarfez-pharmaceuticals-inc).

What drug class is Immediate release torsemide in?

Immediate release torsemide belongs to the Loop diuretic class. See all Loop diuretic drugs at /class/loop-diuretic.

What development phase is Immediate release torsemide in?

Immediate release torsemide is in Phase 2.

What are the side effects of Immediate release torsemide?

Common side effects of Immediate release torsemide include Hypokalemia, Hyponatremia, Dehydration.

What does Immediate release torsemide target?

Immediate release torsemide targets Na-K-2Cl cotransporter 2 (NKCC2) and is a Loop diuretic.

Related

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