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Emetogenic chemotherapy

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

Emetogenic chemotherapy is a Small molecule drug developed by Merck Sharp & Dohme LLC. It is currently in Phase 3 development for Chemotherapy-induced nausea and vomiting (CINV) prevention in patients receiving emetogenic chemotherapy.

Emetogenic chemotherapy refers to chemotherapy agents that induce nausea and vomiting as a side effect, rather than a drug with a specific anti-emetic mechanism.

Emetogenic chemotherapy refers to chemotherapy agents that induce nausea and vomiting as a side effect, rather than a drug with a specific anti-emetic mechanism. Used for Chemotherapy-induced nausea and vomiting (CINV) prevention in patients receiving emetogenic chemotherapy.

Likelihood of approval
64.3% 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.
  • Big-pharma sponsor +3.0pp
    Merck Sharp & Dohme LLC is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
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 nameEmetogenic chemotherapy
SponsorMerck Sharp & Dohme LLC
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Emetogenic chemotherapy is a classification of cytotoxic chemotherapy drugs (such as cisplatin, doxorubicin, and cyclophosphamide) that trigger chemotherapy-induced nausea and vomiting (CINV) through activation of chemoreceptor trigger zones and vagal afferent pathways. This is not a drug itself but rather a category describing the emetogenic potential of various chemotherapy agents used in cancer treatment.

Approved indications

Common side effects

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 Emetogenic chemotherapy

What is Emetogenic chemotherapy?

Emetogenic chemotherapy is a Small molecule drug developed by Merck Sharp & Dohme LLC, indicated for Chemotherapy-induced nausea and vomiting (CINV) prevention in patients receiving emetogenic chemotherapy.

How does Emetogenic chemotherapy work?

Emetogenic chemotherapy refers to chemotherapy agents that induce nausea and vomiting as a side effect, rather than a drug with a specific anti-emetic mechanism.

What is Emetogenic chemotherapy used for?

Emetogenic chemotherapy is indicated for Chemotherapy-induced nausea and vomiting (CINV) prevention in patients receiving emetogenic chemotherapy.

Who makes Emetogenic chemotherapy?

Emetogenic chemotherapy is developed by Merck Sharp & Dohme LLC (see full Merck Sharp & Dohme LLC pipeline at /company/merck).

What development phase is Emetogenic chemotherapy in?

Emetogenic chemotherapy is in Phase 3.

What are the side effects of Emetogenic chemotherapy?

Common side effects of Emetogenic chemotherapy include Nausea, Vomiting, Retching.

Related

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