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23andMe Announces Phase 1 Results from the First-in-Human Phase 1/2a Study of 23ME-00610, an Investigational Antibody Targeting CD200R1

First clinical results to be presented at the AACR Annual Meeting 2023 showed 23ME-00610 demonstrated an acceptable safety and tolerability profile, with favorable pharmacokinetics and peripheral. | April 14, 2023 ....

United States , Head Of Therapeutics Development , American Association For Cancer Research , Eastern Cooperative Oncology Group , Me Holding Co , American Association , Cancer Research , Annual Meeting , Jennifer Low , Therapeutics Development , 23andme Holding Co Stock Exchange , Press Release , Nd Me Us90138q1085 ,

Arrowhead Pharmaceuticals : Complement UK Poster

Safety, Tolerability and Pharmacodynamic Effects of

ARO-C3, a Subcutaneously Administered Investigational

RNAi. | April 3, 2023 ....

Healthy Volunteer Cohorts , Arrowhead Pharmaceuticals , Nc Stock Exchange , Press Release , Dministered Arwr Us04280a1007 ,

Taletrectinib Elicits Durable Responses in TKI-Naïve and Crizotinib-Pretreated ROS1+ NSCLC

Taletrectinib continued to demonstrate meaningful efficacy in the form of a durable objective response rate and a high intracranial ORR with acceptable tolerability in both TKI-naïve and crizotinib-pretreated patients with ROS1-positive non–small cell lung cancer.

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Wei Li , Innovent Biologics Inc , Thoracic Cancer Institute , European Lung Cancer Congress , Tongji University School Of Medicine , Lung Cancer Congress , Medical Oncology , Shanghai Pulmonary Hospital , Tongji University School , Heart Therapeutics , Intracranial Orr , Tki Naïve , Crizotinib Xalkori Pretreated Patients , Ros1 Positive Non Small Cell Lung Cancer , Phase 2 Trusti Trial , 2023 European Lung Cancer Congress ,

BDC-1001 With or Without Nivolumab Shows Early Signs of Clinical Activity, Tolerability in HER2-Expressing Solid Tumors

BDC-1001 monotherapy and in combination with nivolumab generated antitumor activity with acceptable tolerability in patients with advanced HER2-expressing solid tumors, according to topline data from the dose-escalation portion of a phase 1 trial. ....

United States , Editha Perez , Bdc 1001 Monotherapy , Antitumor Activity , Advanced Her2 Expressing Solid Tumors , Dose Escalation Portion Ofa Phase 1 Trial ,

Praxis Precision Medicines' Phase 2 Ulixacaltamide Primary Endpoint Misses Statistical Significance

By Chris Wack

Praxis Precision Medicines Inc. said Friday that topline results from its Phase 2 study evaluating the efficacy, safety and tolerability of ulixacaltamide for the treatment of. | March 3, 2023 ....

United States , Chris Wack , Praxis Precision Medicines Inc , Drug Administration , Precision Medicines , Daily Living , Clinical Global Impression Severity , Patient Global Impression Change , Dow Jones , Praxis Precision Medicines , Nc Stock Exchange , Press Release , Reatment Prax Us74006w1080 ,