Fast Track designation is designed to expedite clinical development and regulatory review timelinesEnrolling patients in the GLEAM trial for ...

Sana Biotechnology (SANA) announced that the U.S. Food and Drug Administration granted Fast Track designation for SC291 in relapsed/refractory systemic lupus erythematosus, which includes extrarenal ...

The U.S. Food and Drug Administration gave SC291, a CD19-directed allogeneic CAR T cell therapy developed using Sana's hypoimmune platform, fast track designation, a process designed to facilitate the ...

Pomerantz LLP is investigating claims on behalf of investors of  Sana Biotechnology, Inc. ("Sana" or the "Company") . Such investors are advised to contact Danielle Peyton at [email protected] or ...

Sana Biotechnology, Inc.'s stock has dropped, but with pipeline focus and upcoming trial data, its prospects remain mixed ...

Under plans to extend the company’s cash runway into 2026, Sana said it has halted development of its CD19-directed allogeneic CAR T-cell therapy, dubbed SC291, in cancer and will instead focus ...

The company is now concentrating its resources on advancing SC291, its anti-CD19 allogeneic CAR-T therapy, for the treatment of B-cell mediated autoimmune diseases (AID). This new focus has led to ...

DelveInsight's 'Follicular Lymphoma Pipeline Insight 2024' report provides comprehensive global coverage of pipeline ...

The company is now concentrating its resources on advancing SC291, its anti-CD19 allogeneic CAR-T therapy, for the treatment of B-cell mediated autoimmune diseases (AID). This new focus has led to the ...

[Click here for information about joining the class action] On November 4, 2024, Sana issued a press release announcing that it "will suspend development of both SC291 in oncology and of SC379 ...

NEW YORK, Nov. 25, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Sana Biotechnology, Inc. ("Sana" or the "Company") (NASDAQ: SANA). Such investors are ...