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chiglitazar sodium tablets

Chipscreen Biosciences, Ltd. · Phase 2 active Small molecule Quality 40/100

chiglitazar sodium tablets is a PPAR agonist Small molecule drug developed by Chipscreen Biosciences, Ltd.. It is currently in Phase 2 development. Also known as: Bilessglu®, CS-038, Carfloglitazar.

Chiglitazar acts as a pan-PPAR agonist, activating all three PPAR subtypes (alpha, gamma, and delta) to regulate glucose and lipid metabolism.

Likelihood of approval
15.3% 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).
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 namechiglitazar sodium tablets
Also known asBilessglu®, CS-038, Carfloglitazar
SponsorChipscreen Biosciences, Ltd.
Drug classPPAR agonist
ModalitySmall molecule
PhasePhase 2

Mechanism of action

Chiglitazar is a balanced pan-PPAR agonist that simultaneously activates PPAR-alpha, PPAR-gamma, and PPAR-delta receptors. This multi-target approach aims to improve insulin sensitivity, reduce blood glucose levels, and favorably modulate lipid profiles while potentially minimizing side effects associated with selective PPAR agonists.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about chiglitazar sodium tablets

What is chiglitazar sodium tablets?

chiglitazar sodium tablets is a PPAR agonist drug developed by Chipscreen Biosciences, Ltd..

How does chiglitazar sodium tablets work?

Chiglitazar acts as a pan-PPAR agonist, activating all three PPAR subtypes (alpha, gamma, and delta) to regulate glucose and lipid metabolism.

Who makes chiglitazar sodium tablets?

chiglitazar sodium tablets is developed by Chipscreen Biosciences, Ltd. (see full Chipscreen Biosciences, Ltd. pipeline at /company/chipscreen-biosciences-ltd).

Is chiglitazar sodium tablets also known as anything else?

chiglitazar sodium tablets is also known as Bilessglu®, CS-038, Carfloglitazar.

What drug class is chiglitazar sodium tablets in?

chiglitazar sodium tablets belongs to the PPAR agonist class. See all PPAR agonist drugs at /class/ppar-agonist.

What development phase is chiglitazar sodium tablets in?

chiglitazar sodium tablets is in Phase 2.

Related

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