OnCo
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Trastuzumab duocarmazine

A HER2 ADC with a DNA-alkylating payload that beat chemotherapy in a phase 3 trial yet never reached the market, because eye and lung toxicity and a stronger rival arrived first.

Byondis' duocarmycin-payload HER2 ADC improved PFS over physician's choice in pretreated HER2+ metastatic breast cancer (TULIP, 2021; PFS 7.0 vs 4.9 months) but with frequent ocular toxicity (~78%) and ILD. The FDA issued a complete response letter in 2023; the EMA application was withdrawn in 2024. Trastuzumab deruxtecan's DESTINY-Breast03 result made its niche disappear.

Lesson: statistical significance is not enough when a competitor redefines the standard; payload toxicity profile decides whether an ADC survives.

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Payload: seco-DUBA (duocarmycin prodrug)
PubChem
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Antibody-drug conjugate (ADC)
Modality
ADC
Mechanism
Trastuzumab with seco-DUBA duocarmycin via cleavable Val-Cit linker; DNA alkylation.
Brand / code
SYD985
Payload
seco-DUBA (duocarmycin)
Linker
Val-Cit cleavable

Trials

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Recruiting now (live from ClinicalTrials.gov)

Recruiting trials near you · live from ClinicalTrials.gov
Trastuzumab duocarmazine
intervention: Trastuzumab duocarmazine
Open on ClinicalTrials.gov →

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Latest papers

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Literature trend2 papers in the last 12 monthsHow this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this drug: (TITLE:"Trastuzumab duocarmazine" OR ABSTRACT:"Trastuzumab duocarmazine" OR TITLE:"SYD985" OR ABSTRACT:"SYD985") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Trastuzumab duocarmazine, not a curated reading list.

Connected

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