Trastuzumab emtansine - Immunogen/Roche
Alternative Names: Ado-trastuzumab emtansine; DM1-trastuzumab immunoconjugate; Herceptin-DM1; Kadcyla; PRO-132365; R3502; RG 3502; RG3502-10; RO 5304020; T-DM1; Trastuzumab-DM1; Trastuzumab-DM1 immunoconjugate; Trastuzumab-MCC-DM1; Trastuzumab-MCC-DM1 antibody-drug conjugate; Trastuzumab–SMCC–DM1 conjugateLatest Information Update: 29 Jul 2024
Price :
$50 *
At a glance
- Originator Genentech; ImmunoGen
- Developer Chugai Pharmaceutical; Dana-Farber Cancer Institute; Genentech; Memorial Sloan-Kettering Cancer Center; Roche; University College London
- Class Antineoplastics; Drug conjugates; Immunotoxins; Macrolides; Maytansinoids; Monoclonal antibodies
- Mechanism of Action Apoptosis stimulants; Mitosis inhibitors; Tubulin inhibitors; Tubulin polymerisation inhibitors
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Marketed HER2 positive breast cancer
- Phase II/III Gastric cancer
- Phase II Bladder cancer; Lung cancer; Non-small cell lung cancer; Salivary gland cancer; Solid tumours; Urogenital cancer
Most Recent Events
- 19 Jun 2024 Roche completes phase-III clinical trials in HER2-positive-breast-cancer (Late-stage disease, Metastatic disease, Combination therapy, Second-line therapy or greater) in USA, United Kingdom, Turkey, Spain, Slovenia, Portugal, Poland, Russia, South Korea, Philippines, Norway, Italy, Greece, France, Finland, Croatia, Colombia, China, Canada, Brazil, Australia (IV) (NCT04740918)
- 23 May 2024 Roche completes a phase III trial in Breast cancer (Adjuvant therapy, Combination therapy, Early-stage disease) in US, EU, Asia, Hong- Kong, Israel, Russia, Taiwan, Turkey, UK, Central and South America, Serbia, South Africa and Switzerland (NCT01772472)
- 09 May 2024 Roche announces intention to submit regulatory filing for Breast cancer (Adjuvant therapy, Combination therapy) in or after 2027 (Roche pipeline, May 2024)