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CKD-843 dose#2
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.
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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).
| 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 name | CKD-843 dose#2 |
|---|---|
| Sponsor | Chong Kun Dang Pharmaceutical |
| Drug class | PPAR-gamma agonist |
| Target | PPAR-gamma |
| Modality | Small molecule |
| Therapeutic area | Metabolic/Endocrinology |
| Phase | Phase 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
- Type 2 diabetes mellitus
Common side effects
- Weight gain
- Fluid retention/edema
- Hypoglycemia
Key clinical trials
- A Phase 3 Study to Evaluate the Safety and Efficacy of CKD-843 in Male Patients With Androgenetic Alopecia (PHASE3)
- The Parallel Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of CKD-843 A (PHASE1)
- A Clinical Traial to Assess Pharmacokinetic/Pharmacodynamic Profiles and Safety of CKD-843 (PHASE1)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- CKD-843 dose#2 CI brief — competitive landscape report
- CKD-843 dose#2 updates RSS · CI watch RSS
- Chong Kun Dang Pharmaceutical portfolio CI
Frequently asked questions about CKD-843 dose#2
What is CKD-843 dose#2?
How does CKD-843 dose#2 work?
What is CKD-843 dose#2 used for?
Who makes CKD-843 dose#2?
What drug class is CKD-843 dose#2 in?
What development phase is CKD-843 dose#2 in?
What are the side effects of CKD-843 dose#2?
What does CKD-843 dose#2 target?
Related
- Drug class: All PPAR-gamma agonist drugs
- Target: All drugs targeting PPAR-gamma
- Manufacturer: Chong Kun Dang Pharmaceutical — full pipeline
- Therapeutic area: All drugs in Metabolic/Endocrinology
- Indication: Drugs for Type 2 diabetes mellitus
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing