^
Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Go to data
Title:

PF-06804103 Dose Escalation in HER2 Positive and Negative (Negative Only in Part 2) Solid Tumors

Excerpt:
...- HER2 positive breast cancer or gastric cancer that is resistant to standard therapy or for which...
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Title:

A phase I dose escalation study evaluating the safety and tolerability of a novel anti-HER2 antibody-drug conjugate (PF-06804103) in patients with HER2-positive solid tumors.

Excerpt:
In Part 1, groups of adult patients (pts) with HER2+ BC or HER2+ GC, who are resistant or intolerant to standard therapy or for which no standard therapy is available, received PF-06804103 intravenously once every 21 days (Q3W)...Preliminary ORR in the patients treated with doses ≥3mg/kg was 52.4% (11/21)....The PF-06804103 ADC demonstrated manageable toxicity and promising anti-tumor activity in this small, heavily pretreated study population.
DOI:
10.1200/JCO.2020.38.15_suppl.1039
Trial ID: