Rubius Therapeutics Inc RUBY stock is trading after reporting initial data from its ongoing Phase 1/2 trial of RTX-240 in patients with advanced solid tumors.
- Initial efficacy results showed a confirmed partial response (PR) with a 54% reduction in the target lesions in a patient with metastatic anal cancer whose disease had progressed on anti-PD-L1 therapy.
- Stable disease (SD) was observed in six patients, including four patients with stable disease for at least 12 weeks.
- The most common treatment-related mild/moderate adverse events were fatigue, chills, nausea, decreased appetite, and arthralgias on the safety front.
- No treatment-related severe/serious adverse events, no dose-limiting toxicities, and a single Grade 1 event of liver toxicity were reported.
- Trafficking of T and NK cells into the tumor microenvironment was observed in 3/5 patients (1.6 to 10-fold increases).
- In one patient with acute myeloid leukemia, trafficking of T and NK cells into the bone marrow was associated with increases in the marrow's cellularity.
- The company plans to initiate a Phase 1 trial of RTX-240 combined with anti-PD-1 therapy in advanced solid tumors in the second half of this year.
- Initial data from RTX-321 for the treatment of HPV 16-positive cancers are expected by Q1 of 2022.
- The company plans to submit an Investigational New Drug Application for RTX-224 by year-end.
- HC Wainwright raised the price target on Rubius Therapeutics from $28 to $40.
- Price Action: RUBY shares were trading 79.1% higher at $29.40 in market trading hours.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in