BRIEF-Medicenna Presents Updated Results Of Single Agent MDNA11 Anti-Tumor Activity From Dose Escalation And Ongoing Dose Expansion Of The Phase 1/2 ABILITY-1 Study At The 2024 Annual Meeting Of The American Association For Cancer Research

Reuters04-10

April 9 (Reuters) - Medicenna Therapeutics Corp

:

* MEDICENNA PRESENTS UPDATED RESULTS OF SINGLE AGENT MDNA11 ANTI-TUMOR ACTIVITY FROM DOSE ESCALATION AND ONGOING DOSE EXPANSION OF THE PHASE 1/2 ABILITY-1 STUDY AT THE 2024 ANNUAL MEETING OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH (AACR)

* MEDICENNA THERAPEUTICS CORP - DURABLE STABLE DISEASE $(SD)$ IN 3 MELANOMA PATIENTS FOR 6 TO 18 MONTHS WITH CONCOMITANT TUMOR SHRINKAGE

* MEDICENNA THERAPEUTICS CORP - MDNA11 IS GENERALLY WELL TOLERATED WITH NO DOSE-LIMITING TOXICITIES OR VASCULAR LEAK SYNDROME REPORTED IN ANY OF DOSE ESCALATION COHORTS

* MEDICENNA THERAPEUTICS CORP - 100% REDUCTION OF TARGET LESIONS IN ONE MELANOMA AND ONE PANCREATIC CANCER PATIENT OBSERVED AMONG 4 PR TO DATE

* MEDICENNA THERAPEUTICS - NEW SITES IN US & KOREA STARTED ENROLMENT IN ONGOING MONOTHERAPY EXPANSION & COMBINATION ESCALATION ARMS OF ABILITY-1 STUDY

Source text for Eikon: Further company coverage:

((Reuters.Briefs@thomsonreuters.com;))

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Comments

We need your insight to fill this gap
Leave a comment