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rhprouk

Suzhou RxD Biopharmaceutical Co., Ltd · Phase 3 active Small molecule ✓ Verified May 2026

rhprouk is a Small molecule drug developed by Suzhou RxD Biopharmaceutical Co., Ltd. It is currently in Phase 3 development. Also known as: Controlled.

Rhprouk is being studied in a Phase III clinical trial for the treatment of STEMI (ST Elevated Myocardial Infarction) patients in China. The trial, NCT02367976, is being conducted by Suzhou RxD Biopharmaceutical Co., Ltd.

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 namerhprouk
Also known asControlled
SponsorSuzhou RxD Biopharmaceutical Co., Ltd
ModalitySmall molecule
Therapeutic areaOther
PhasePhase 3

Approved indications

No approved indications tracked.

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 rhprouk

What is rhprouk?

rhprouk is a Small molecule drug developed by Suzhou RxD Biopharmaceutical Co., Ltd.

Who makes rhprouk?

rhprouk is developed by Suzhou RxD Biopharmaceutical Co., Ltd (see full Suzhou RxD Biopharmaceutical Co., Ltd pipeline at /company/suzhou-rxd-biopharmaceutical-co-ltd).

Is rhprouk also known as anything else?

rhprouk is also known as Controlled.

What development phase is rhprouk in?

rhprouk is in Phase 3.

Related

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