Drug · Small Molecule
Etoposide
CI-DRUG-00000225Explore in graph →NCIt C491 CHEMBL44657 CIViC Approved
Regulatory
Approvals (18)
Each record names the authority, jurisdiction, indication text and status. A drug approved in one jurisdiction for one indication is not 'approved' in general.
- Source
- Health Canada — Drug Product Database (DPD)
- Dataset
- Health Canada DPD
- Version
- dpd-2026-09-11
- Retrieved
- Sep 11, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- regulatory
- License
- Open Government Licence – Canada (https://open.canada.ca/en/open-government-licence-canada)
- Run
- ING-HEALTHCANADADPD-20260911-000001
| Jurisdiction · authority | Cancer | Indication | Status | Approval date | Source |
|---|---|---|---|---|---|
| CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION (DIN 02552671) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | approvedsource: Marketed | Jun 20, 2025 | health-canada-dpd |
| CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION (DIN 02239961) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormantsince Aug 3, 2017 | Oct 20, 2014 | health-canada-dpd |
| CA Health Canada | — | Marketed in Canada as ETOPOSIDE INJECTION, USP (DIN 02422530) under ATC L01CB01 ETOPOSIDE. Indications are not published in the Drug Product Database — see the Health Canada Product Monograph. | withdrawnsource: Dormant |
Health Canada records are DIN-level: one row per marketed product (brand, strength, form). The Drug Product Database does not publish indications, so no cancer is stated for these rows, and a cancelled or dormant DIN is the status of that one product — not a withdrawal of the molecule.
Data updated 18 hours agoSource updated unknown
Derived
Development pipeline
Most advanced stage across all cancers, then per top-level cancer reached through trial conditions or approval indications. Approval in any ingested jurisdiction outranks trial phase; counts are interventional studies.
| Scope | Stage | Max phase | Active | Recruiting | Phase 3 | Trials | Approvals | Jurisdictions | First approval | First trial |
|---|---|---|---|---|---|---|---|---|---|---|
| All cancers | Approved | Phase 4 | 239 | 110 | 283 | 1,194 | 18 | CA, US | Dec 31, 1984 | 1988-03 |
| Malignant Lung Neoplasm | Approved | Phase 4 | 58 | 25 | 51 | 219 | 3 | US | Dec 30, 1986 | 1993-01 |
| Malignant Testicular Neoplasm | Approved | Phase 3 | 2 | 1 | 3 | 10 | 1 | US | Feb 13, 2026 | Nov 3, 2003 |
| Non-Hodgkin Lymphoma | Phase4 | Phase 4 | 48 | 20 | 30 | 200 | 0 |
Curated evidence
Clinical evidence (10)
CIViC items in which this therapy appears, grouped by cancer context, then molecular profile. 50 items per page.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 15659725
- Run
- ING-CIVIC-20260908-000001
| Therapy | Cancer | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| NPM1 W288FS1 | ||||||||
| Cytarabine + Daunorubicin | ||||||||
Clinical trials
Trials with this intervention (1,197)
Most recently updated first, 50 per page.
- Source
- ClinicalTrials.gov
- Dataset
- ClinicalTrials.gov API v2 studies
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
| NCT | Title | Status | Phase | Enrollment (n) | Sponsor | Countries | Last update | Source |
|---|---|---|---|---|---|---|---|---|
| NCT00092222 | Virotherapy and Natural History Study of KHSV-Associated Multricentric Castleman s Disease With Correlates of Disease Activity | active not recruiting | Phase 2 | 75 | National Cancer Institute (NCI)NIH | 1 | Sep 28, 2026 | clinicaltrials |
| NCT03418038 | Ascorbic Acid and Chemotherapy for the Treatment of Relapsed or Refractory Lymphoma, CCUS, and Chronic Myelomonocytic Leukemia |