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Paraplatin

ARCAGY/ GINECO GROUP · Phase 3 active Small molecule Under review

Paraplatin is a Small molecule drug developed by ARCAGY/ GINECO GROUP. It is currently in Phase 3 development for Breast cancer, Malignant tumor of ovary. Also known as: carboplatin.

Paraplatin, also known as carboplatin, is a chemotherapy medication used to treat various forms of cancer, including ovarian cancer, as well as other types such as lung cancer, head and neck cancer, brain cancer, and neuroblastoma. It is administered by injection into a vein.

Likelihood of approval
61.3% 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).
  • Oncology Phase 3 boost +3.0pp
    Oncology Phase 3 trials have higher approval rates (~61%) than the cross-industry average due to clearer endpoints and FDA oncology pathway.
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 nameParaplatin
Also known ascarboplatin
SponsorARCAGY/ GINECO GROUP
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

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 Paraplatin

What is Paraplatin?

Paraplatin is a Small molecule drug developed by ARCAGY/ GINECO GROUP, indicated for Breast cancer, Malignant tumor of ovary.

What is Paraplatin used for?

Paraplatin is indicated for Breast cancer, Malignant tumor of ovary.

Who makes Paraplatin?

Paraplatin is developed by ARCAGY/ GINECO GROUP (see full ARCAGY/ GINECO GROUP pipeline at /company/arcagy-gineco-group).

Is Paraplatin also known as anything else?

Paraplatin is also known as carboplatin.

What development phase is Paraplatin in?

Paraplatin is in Phase 3.

Related

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