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CKD-843 dose#2

Chong Kun Dang Pharmaceutical · Phase 3 active Small molecule Under review

CKD-843 dose#2 is a PPAR-gamma agonist Small molecule drug developed by Chong Kun Dang Pharmaceutical. It is currently in Phase 3 development for Type 2 diabetes mellitus.

CKD-843 is a selective PPAR-gamma agonist that enhances insulin sensitivity and reduces inflammation.

CKD-843 dose #2 is part of a clinical trial studying the pharmacokinetic/pharmacodynamic profiles and safety of CKD-843 in patients with alopecia and androgenetic alopecia. The trial involves interventions CKD-843 A, CKD-843 B, and CKD-843-R, but the specific details of CKD-843 dose #2 are not provided in the available information.

Likelihood of approval
58.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% 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 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +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 nameCKD-843 dose#2
SponsorChong Kun Dang Pharmaceutical
Drug classPPAR-gamma agonist
TargetPPAR-gamma
ModalitySmall molecule
Therapeutic areaMetabolic/Endocrinology
PhasePhase 3

Mechanism of action

PPAR-gamma agonists activate peroxisome proliferator-activated receptor gamma, a nuclear receptor involved in glucose metabolism and anti-inflammatory signaling. By binding to PPAR-gamma, CKD-843 improves insulin sensitivity in peripheral tissues and reduces systemic inflammation, making it potentially useful in metabolic and inflammatory conditions. This mechanism is characteristic of the thiazolidinedione drug class.

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

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

Frequently asked questions about CKD-843 dose#2

What is CKD-843 dose#2?

CKD-843 dose#2 is a PPAR-gamma agonist drug developed by Chong Kun Dang Pharmaceutical, indicated for Type 2 diabetes mellitus.

How does CKD-843 dose#2 work?

CKD-843 is a selective PPAR-gamma agonist that enhances insulin sensitivity and reduces inflammation.

What is CKD-843 dose#2 used for?

CKD-843 dose#2 is indicated for Type 2 diabetes mellitus.

Who makes CKD-843 dose#2?

CKD-843 dose#2 is developed by Chong Kun Dang Pharmaceutical (see full Chong Kun Dang Pharmaceutical pipeline at /company/chong-kun-dang-pharmaceutical).

What drug class is CKD-843 dose#2 in?

CKD-843 dose#2 belongs to the PPAR-gamma agonist class. See all PPAR-gamma agonist drugs at /class/ppar-gamma-agonist.

What development phase is CKD-843 dose#2 in?

CKD-843 dose#2 is in Phase 3.

What are the side effects of CKD-843 dose#2?

Common side effects of CKD-843 dose#2 include Weight gain, Fluid retention/edema, Hypoglycemia.

What does CKD-843 dose#2 target?

CKD-843 dose#2 targets PPAR-gamma and is a PPAR-gamma agonist.

Related

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