- I-Mab IMAB unveiled early results from Phase 1 study evaluating uliledlimab in combination with Roche Holdings AG’s RHHBY Tecentriq (atezolizumab) in patients with advanced cancer.
- An abstract detailing data from the trial will be presented at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, taking place next month.
- I-Mab touted a 23% objective response rate and disease control rate of 46% in the study among 13 evaluable patients with several different types of advanced cancers.
- A patient with ovarian cancer achieved a complete response; two others saw a partial response, while three had stable disease.
- In particular, investigators reported no “hook effect” in the Phase I trial, meaning the antibody potency seemed to increase proportionately with the dose rather than losing inhibition at a higher dose, an issue observed with certain other drugs in the class.
- The clinical activity was observed in both PD-(L)1 treatment naïve and refractory cancer patients, including one partial response patient who previously failed Bristol-Myers Squibb Co’s BMY Opdivo (nivolumab).
- The combination was safe and well-tolerated with no dose-limiting toxicity. All treatment-related adverse events were either mild or moderate.
- Price Action: IMAB shares closed at $63.46 on Wednesday.
Loading...
Loading...
BMYBristol-Myers Squibb Co
$46.010.17%
Edge Rankings
Momentum
26.25
Growth
59.07
Quality
36.23
Value
33.57
Price Trend
Short
Medium
Long
© 2025 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.