Phase I study of IPN60090 in patients with advanced solid tumors
MD Anderson Study Status
IPN60090, pembrolizumab, paclitaxel, IPN60090 single administration
The purpose of the protocol is to determine safety, tolerability, recommended dose (RD), pharmacokinetics (PK), pharmacodynamics (PD) and preliminary anti-tumour activity of IPN60090 as a single agent (Part A) and in combination with pembrolizumab (Part B) or paclitaxel (Part C) in patients with advanced solid tumours and to evaluate food effect (Part D).
Resources and Links
Phone Number: 1-877-MDA-6789
Information and next steps
Investigational Cancer Therapeutics
For general questions about clinical trials:
Due to our response to COVID-19, all blood donations at MD Anderson
Blood Donor Center locations are being held by appointment only.