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ABP-745 Dose B
ABP-745 Dose B is a Small molecule drug developed by Atom Therapeutics Co., Ltd. It is currently in Phase 2 development.
ABP-745 Dose B is a small molecule intervention being studied in a clinical trial for conditions including acute gouty arthritis and atherosclerosis cardiovascular disease. The study, NCT07145229, is a randomized, double-blind, multicenter trial comparing ABP-745 Dose B to colchicine in participants with an acute gout flare.
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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).
| 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 name | ABP-745 Dose B |
|---|---|
| Sponsor | Atom Therapeutics Co., Ltd |
| Modality | Small molecule |
| Phase | Phase 2 |
Approved indications
Common side effects
Key clinical trials
- Efficacy, Safety, and PopPK Profile of ABP-745 in Patients With Atherosclerosis (PHASE2)
- Safety and Efficacy of ABP-745 in Participants With an Acute Gout Flare (PHASE2)
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:
- ABP-745 Dose B CI brief — competitive landscape report
- ABP-745 Dose B updates RSS · CI watch RSS
- Atom Therapeutics Co., Ltd portfolio CI
Frequently asked questions about ABP-745 Dose B
What is ABP-745 Dose B?
Who makes ABP-745 Dose B?
What development phase is ABP-745 Dose B in?
Related
- Manufacturer: Atom Therapeutics Co., Ltd — full pipeline
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing