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Takecab

Genuine Research Center, Egypt · Phase 1 active Small molecule ✓ Verified May 2026

Takecab is a Small molecule drug developed by Genuine Research Center, Egypt. It is currently in Phase 1 development for Duodenal ulcer disease, Gastric ulcer, Gastro-esophageal reflux disease with esophagitis.

Vonoprazan, a small molecule, is used to treat various gastrointestinal conditions, including Reflux Esophagitis, Gastroesophageal Reflux Disease, and Gastric/Duodenal Ulcer, among others. It is administered in combination with Amoxicillin 500 mg tid, as seen in clinical trials such as NCT03214081.

Likelihood of approval
11.6% vs 9.6% industry baseline
If approved by FDA: likely 2033–2036
Steps remaining: Phase 2 → Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 1 → approval rate +9.6pp
    Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Anti-infectives pathway favourability +2.0pp
    Microbiological endpoints + non-inferiority designs raise approval rates above baseline.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2033–2036
EMA EU 2034–2037 +0.7 yr
MHRA GB 2034–2037 +0.7 yr
Health Canada CA 2034–2038 +0.9 yr
TGA AU 2034–2038 +1.2 yr
PMDA JP 2034–2038 +1.5 yr
NMPA CN 2035–2039 +2.3 yr
MFDS KR 2034–2038 +1.4 yr
CDSCO IN 2034–2039 +1.8 yr
ANVISA BR 2035–2039 +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 nameTakecab
SponsorGenuine Research Center, Egypt
TargetPotassium-transporting ATPase
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 1

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 Takecab

What is Takecab?

Takecab is a Small molecule drug developed by Genuine Research Center, Egypt, indicated for Duodenal ulcer disease, Gastric ulcer, Gastro-esophageal reflux disease with esophagitis.

What is Takecab used for?

Takecab is indicated for Duodenal ulcer disease, Gastric ulcer, Gastro-esophageal reflux disease with esophagitis, Infection caused by Helicobacter pylori.

Who makes Takecab?

Takecab is developed by Genuine Research Center, Egypt (see full Genuine Research Center, Egypt pipeline at /company/genuine-research-center-egypt).

What development phase is Takecab in?

Takecab is in Phase 1.

What does Takecab target?

Takecab targets Potassium-transporting ATPase.

Related

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