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| Therapy Name | Capecitabine + IAM1363 + Zanidatamab |
| Synonyms | |
| Therapy Description | |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| Capecitabine | Xeloda | R340|Ro 09-1978/000 | Chemotherapy - Antimetabolite 14 | Xeloda (capecitabine) is a prodrug that is converted to 5-FU, ultimately inhibiting RNA and DNA synthesis and cell division (PMID: 28520372). Xeloda (capecitabine) is FDA-approved for use in patients with colorectal, breast, gastric, esophageal, gastroesophageal junction, and pancreatic cancer (FDA.gov). |
| IAM1363 | IAM-H1|ENT-H1 | HER2 Inhibitor 45 | IAM1363 irreversibly inhibits wild-type and mutant ERBB2 (HER2), including exon 20 insertions, potentially leading to tumor growth inhibition (Cancer Res (2023) 83 (7_Supplement): 4034). | |
| Zanidatamab | Ziihera | ZW-25|ZW25|Zanidatamab-hrii | HER2 (ERBB2) Antibody 80 | Ziihera (zanidatamab) is a bispecific antibody targeting ERBB2 (HER2), which induces anti-tumor immune response against Erbb2 (Her2)-expressing tumors (Ann Oncol 2017, Vol 28, Suppl 5, Abstract # 255P, PMID: 32054397). Ziihera (zanidatamab) is FDA-approved for use in patients with unresectable or metastatic ERBB2 (HER2)-positive (IHC 3+) biliary tract cancer (FDA.gov). |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
|---|---|---|---|---|---|---|
| NCT06253871 | Phase I | IAM1363 IAM1363 + Pembrolizumab Carboplatin + IAM1363 + Pembrolizumab + Pemetrexed Disodium Capecitabine + IAM1363 + Trastuzumab Capecitabine + IAM1363 + Zanidatamab IAM1363 + Trastuzumab deruxtecan | A Phase 1/1b Study of IAM1363 in HER2 Cancers | Recruiting | USA | NLD | ITA | IRL | GBR | FRA | ESP | 1 |