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Health care stocks were decreasing late Friday afternoon, with the NYSE Health Care Index easing 0.2% and the Health Care Select Sector SPDR Fund (XLV) shedding 0.3%.
The iShares Biotechnology ETF (IBB) was fractionally lower.
In corporate news, Estrella Immunopharma shares rose 2% after the firm said it has completed the first dose group in an ongoing phase 1/2 trial assessing EB103 in adults with relapsed/refractory B-cell non-Hodgkin lymphoma.
Bluebird bio shares plunged 42% after it agreed to be acquired by funds managed by Carlyle (CG) and SK Capital Partners.
UnitedHealth Group on Friday refuted a report by The Wall Street Journal that the US Department of Justice started an investigation into the health insurer's Medicare billing practices. UnitedHealth shares fell 7.3%.
Novo Nordisk resolved its shortage of weight-loss drugs Ozempic and Wegovy, according to an update on the US Food and Drug Administration website. Companies such as Hims & Hers Health will no longer be legally allowed to make and sell compounded alternatives. Novo Nordisk shares jumped 5.4%, while Hims & Hers tumbled 24%.
Health care stocks were softer late Friday afternoon with the NYSE Health Care Index easing 0.2% and the Health Care Select Sector SPDR Fund (XLV) down 0.3%.
The iShares Biotechnology ETF (IBB) was fractionally lower.
In corporate news, Estrella Immunopharma shares climbed 3.4% after it said Friday it has completed the first dose group in an ongoing phase 1/2 trial assessing EB103 in adults with relapsed/refractory B-cell non-Hodgkin lymphoma.
(16:58 GMT) Estrella Immunopharma Price Target Maintained With a $16.00/Share by D. Boral Capital
Estrella Immunopharma said Friday it has completed the first dose group in its ongoing phase I/II clinical trial evaluating EB103 in adult patients with relapsed/refractory B-cell non-Hodgkin lymphoma.
Based on preliminary data, no dose-limiting toxicities or serious adverse events related to treatment were observed in the group, with tumor response noted in all patients in the first month, the company said.
After reviewing safety and efficacy data, the Data and Safety Monitoring Board has approved the initiation of a higher dose group, the company added.
The company's shares were up 4% in recent trading.
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