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BridgeBio Pharma : BBIO – Acoramidis AG10 TTR – ISA 2024 – Acoramidis treatment related increase in serum TTR is associated with lower cardiovascular mortality in ATTR CM

Treatment-Related Early Increase in Serum TTR is Associated With Lower Cardiovascular Mortality in ATTR-CM: Insights From ATTRibute-CM Amrut.

United statesUnited kingdomNew yorkCzech republicUniversity collegeNew south walesUniversity of chicagoSan franciscoRegion flamandeSouth australiaSanta monicaUniversity of texas southwestern medical centerCity ofRichard wrightMatthias dupontSatish rao

BridgeBio Pharma : BBIO – Acoramidis AG10 TTR – ISA 2024 – Early increase in serum transthyretin level is an independent predictor of improved survival in ATTR cardiomyopathy

Early Increase in Serum Transthyretin Level Is an Independent Predictor of Improved Survival in ATTR Cardiomyopathy: Insights From Acoramidis Phase 3 Study ATTRibute-CM .

San franciscoUnited statesNoord hollandNew yorkUniversity of chicagoColumbia universitySteen hvitfeldt poulsenBrian adamKuma sinhaSurendhar reddy chepyalaAnique ducharmeSatish raoMathews maurerAmrut ambardekarMartha groganNitasha sarswat

Viking Therapeutics Reports First Quarter 2024 Financial Results and Provides Corporate Update

Viking Therapeutics Reports First Quarter 2024 Financial Results and Provides Corporate Update
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New yorkUnited statesLas vegasObesity health forumTherapeutics incPrnewswire viking therapeutics incDrug administrationLigand pharmaceuticals incorporatedExchange commissionBofa securities health care conferenceTherapeutics reports first quarterProvides corporateFrom phasePlacebo adjusted weight lossFrom baselinePromising safety

Viking Therapeutics Announces Positive Top-Line Results from Phase 2 VENTURE Trial of Dual GLP-1/GIP Receptor Agonist VK2735 in Patients with Obesity

Study Achieves Primary and all Secondary Endpoints, Demonstrating Statistically Significant Reductions in Body Weight at all Doses as Compared to Placebo Up to 13.1% Placebo-Adjusted Mean Weight.

Drug administrationLigand pharmaceuticals incorporatedTherapeutics incStudy achieves primarySecondary endpointsBody weightPlacebo adjusted mean weight lossFrom baselineObserved afterWeek studyTreatment emergent adverse events considered mildCall scheduledViking therapeuticsBody weight followingOnce weekly dosingCommon gastrointestinal

Vertex Announces Positive Results From the VX-548 Phase 3 Program for the Treatment of Moderate-to-Severe Acute Pain

– Treatment with VX-548 led to statistically significant improvement in pain compared to placebo as well as a clinically meaningful reduction in pain from baseline in both the abdominoplasty and.

United statesCity ofUnited kingdomJessica oswaldReshma kewalramaniExchange commissionVertex pharmaceuticals conference callVertex pharmaceuticals incorporated nasdaqCompanies to workDrug administrationVertex pharmaceuticals incorporatedAcute pain following abdominoplastyBusiness wireNumeric pain rating scalePatients undergoingKey secondary outcomes