BRIEF-Palvella Therapeutics Announces Positive Topline Results From Phase 3 Selva Clinical Study Of Qtorin™

Reuters

02/24

BRIEF-<a href="https://laohu8.com/S/PVLA">Palvella Therapeutics</a> Announces Positive Topline Results From Phase 3 Selva Clinical Study Of Qtorin™

Feb 24 (Reuters) - Palvella Therapeutics Inc PVLA.O:

PALVELLA THERAPEUTICS ANNOUNCES POSITIVE TOPLINE RESULTS FROM PHASE 3 SELVA CLINICAL STUDY OF QTORIN™ 3.9% RAPAMYCIN ANHYDROUS GEL (QTORIN™ RAPAMYCIN) IN MICROCYSTIC LYMPHATIC MALFORMATIONS
PALVELLA THERAPEUTICS INC: PALVELLA PLANS TO SUBMIT A NEW DRUG APPLICATION TO FDA IN SECOND HALF OF 2026
PALVELLA THERAPEUTICS INC - PHASE 3 TRIAL MEETS PRIMARY ENDPOINT WITH SIGNIFICANT IMPROVEMENT
PALVELLA THERAPEUTICS INC - QTORIN™ RAPAMYCIN WELL-TOLERATED WITH NO SERIOUS ADVERSE EVENTS
PALVELLA - ACHIEVED STATISTICAL SIGNIFICANCE ON PRE-SPECIFIED KEY SECONDARY ENDPOINT (P<0.001) & ALL 4 SECONDARY EFFICACY ENDPOINTS (ALL P<0.001)

Source text: ID:nGNX6zqMf0

Further company coverage: PVLA.O

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

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ALL 4 SECONDARY EFFICACY ENDPOINTS (ALL P&lt;0.001)</p></li></ul><p>Source text: <span>ID:nGNX6zqMf0</span></p><p>Further company coverage: <span>PVLA.O</span></p><p> ((Reuters.Briefs@thomsonreuters.com;))</p></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"PVLA","symbol_name":"Palvella Therapeutics","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260224:nTUA8GSX1W:1","article_id":"2613713352","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2613713352","pubTimestamp":1771933039,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"BRIEF-Palvella Therapeutics Announces Positive Topline Results From Phase 3 Selva Clinical Study Of QtorinFeb 24 (Reuters) - Palvella Therapeutics Inc PVLA.O:PALVELLA THERAPEUTICS ANNOUNCES POSITIVE T","collect":0,"end_time":0,"defaultTopTitle":"","property":[],"viewcount":null,"language":"en","relate_stocks":{"PVLA":"Palvella Therapeutics","BK4139":"生物科技"},"translate_title":"简介-Palvella Therapeutics宣布Qtorin 3期Selva临床研究的积极顶线结果™","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"PVLA":0.9},"content_text":"BRIEF-Palvella Therapeutics Announces Positive Topline Results From Phase 3 Selva Clinical Study Of Qtorin™Feb 24 (Reuters) - Palvella Therapeutics Inc PVLA.O:PALVELLA THERAPEUTICS ANNOUNCES POSITIVE TOPLINE RESULTS FROM PHASE 3 SELVA CLINICAL STUDY OF QTORIN™ 3.9% RAPAMYCIN ANHYDROUS GEL (QTORIN™ RAPAMYCIN) IN MICROCYSTIC LYMPHATIC MALFORMATIONSPALVELLA THERAPEUTICS INC: PALVELLA PLANS TO SUBMIT A NEW DRUG APPLICATION TO FDA IN SECOND HALF OF 2026PALVELLA THERAPEUTICS INC - PHASE 3 TRIAL MEETS PRIMARY ENDPOINT WITH SIGNIFICANT IMPROVEMENTPALVELLA THERAPEUTICS INC - QTORIN™ RAPAMYCIN WELL-TOLERATED WITH NO SERIOUS ADVERSE EVENTSPALVELLA - ACHIEVED STATISTICAL SIGNIFICANCE ON PRE-SPECIFIED KEY SECONDARY ENDPOINT (P<0.001) & ALL 4 SECONDARY EFFICACY ENDPOINTS (ALL P<0.001)Source text: ID:nGNX6zqMf0Further company coverage: PVLA.O ((Reuters.Briefs@thomsonreuters.com;))","kind":"highlight","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"1","news_tag":"productRelease","news_rank":0,"symbols":[],"gpt_button":0,"need_auth":true,"code":"91000000","status":"200"}}}