Sept 24 (Reuters) - Lidds AB LIDDS.ST :
* REG-PRELIMINARY RESULTS FROM PHASE IIB LIPROCA® DEPOT
DOSE-FINDING STUDY SHOW A STRONG MAXIMUM PSA DECREASE AND
SUSTAINED PSA REDUCTION EFFECT
* LIDDS - PSA REDUCTION FOR PART II PATIENTS WAS IN LINE
WITH
EXPECTED PATTERN FOR LIPROCA DEPOT'S SUSTAINED RELEASE AND
MAXIMUM PSA REDUCTION (PSA NADIR) OCCURRED DURING MONTHS 2-4
* PATIENTS IN PART II SHOWED A STRONG PSA DECREASE AND A
CONTINUED
PSA REDUCTION AT MONTH 5 AS WELL AS OVER FULL STUDY PERIOD OF
SIX MONTHS, CONFIRMING NANOZOLID® TECHNOLOGY'S SUSTAINED RELEASE
PROFILE
* POSITIVE PRELIMINARY RESULTS SHOW LIPROCA® DEPOT'S ABILITY
TO
REDUCE PSA LEVELS OVER A PERIOD OF SIX MONTHS, PROVING
NANOZOLID® TECHNOLOGY'S SUITABILITY FOR LOCAL CANCER TREATMENT
* STUDY ALSO CONFIRMS TECHNOLOGY'S FAVORABLE TOXICITY AND
TOLERABILITY PROFILE
* LIDDS - LIPROCA DEPOT WAS WELL TOLERATED WITHOUT HORMONAL
SIDE
EFFECTS ASSOCIATED WITH ANTI-ANDROGEN THERAPIES
* LIDDS - MAJORITY OF PATIENTS IN STUDY WERE POSITIVE TO
RECEIVING
A SECOND INJECTION
Source text for Eikon: ID:nGNE3PJG8X
Further company coverage: LIDDS.ST
(Gdynia Newsroom)
((gdynia.newsroom@thomsonreuters.com;))