May 26 (Reuters) - Harpoon Therapeutics Inc HARP.O :
* HARPOON PRESENTS INTERIM DATA FROM ONGOING DOSE ESCALATION
PORTION OF T CELL ENGAGER HPN328 CLINICAL TRIAL AT 2022 ASCO
ANNUAL MEETING
* HARPOON THERAPEUTICS INC - HPN328 CLINICALLY ACTIVE AND
WELL
TOLERATED IN PATIENTS WITH SOLID TUMORS
* HARPOON THERAPEUTICS - FAVORABLE SAFETY PROFILE EMERGING:
22%
OF PATIENTS EXPERIENCED GRADE 1-2 CRS; NO GRADE 3 OR HIGHER CRS
FROM HPN328 TRIAL
* HARPOON THERAPEUTICS - ONE CONFIRMED PARTIAL RESPONSE; 27%
OF
SMALL CELL LUNG CANCER PATIENTS WITH TARGET LESION REDUCTIONS OF
30% OR MORE FROM HPN328 TRIAL
* HARPOON THERAPEUTICS INC - TREATMENT DURATION NOW GREATER
THAN
20 WEEKS IN ONE-THIRD OF PATIENTS
* HARPOON THERAPEUTICS INC - DOSE ESCALATION IS ONGOING;
MAXIMUM
TOLERATED DOSE NOT YET REACHED
* HARPOON THERAPEUTICS - AS OF DATA CUT-OFF DATE OF APRIL
21,
2022, SHOWED THAT HPN328 DEMONSTRATED ANTI-TUMOR ACTIVITY AND A
FAVORABLE SAFETY PROFILE
* HARPOON THERAPEUTICS INC - TO DATE, THERE HAVE BEEN NO
DOSE-LIMITING TOXICITIES OBSERVED AND NO DISCONTINUATIONS DUE TO
ADVERSE EVENTS
Source text for Eikon: ID:nGNX8V6lHK
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