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Iovance Biotherapeutics Announces Clinical Data Updates for Lifileucel in Advanced Melanoma During American Association for Cancer Research (AACR) 2021 Annual Meeting

Published: Apr 09, 2021
Median Duration of Response Not Reached at 28.1 Months of Median Study Follow Up in Cohort 2 of C-144-01 Study
36.4% Overall Response Rate; Continued Deepening of Responses
SAN CARLOS, Calif., April 09, 2021 (GLOBE NEWSWIRE)
Iovance Biotherapeutics, Inc. (NASDAQ: IOVA), a late-stage biotechnology company developing novel T cell-based cancer immunotherapies, today announced data from Cohort 2 in the C-144-01 study of lifileucel in advanced melanoma. These data will be part of an oral presentation in a Clinical Trials Plenary Session at the upcoming American Association for Cancer Research (AACR) 2021 Annual Meeting.
“We are very excited to report our latest Cohort 2 melanoma data in an oral presentation at AACR,” said Maria Fardis, Ph.D., President and Chief Executive Officer of Iovance Biotherapeutics. “The long term follow up data show that median duration of response was not reached at 28.1 months of median study follow u ....

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March 2021 BLS Jobs Situation - Job Gains Excellent For A Second Month In A Row

March 2021 BLS Jobs Situation - Job Gains Excellent For A Second Month In A Row
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Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma

Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma
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STOCKHOLM, March 8, 2021 /PRNewswire/ Oncopeptides AB (publ) (Nasdaq Stockholm: ONCO
), a global biotech company focused on the development of therapies for difficult-to-treat hematological diseases, today announced that it strengthens the leadership of the European operations by appointing Andrea Passalacqua as General Manager in Europe, and Pamela Bacon as Head of Medical Affairs Europe. The Company also announced that it opens an Early Access Program across Europe to address the significant need of new treatment alternatives in multiple myeloma. As previously announced, Oncopeptides will also seek a Conditional Marketing Authorization of melphalan flufenamide in triple class refractory multiple myeloma, during second quarter of 2021. ....

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Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma

Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma
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Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma

Oncopeptides strengthens leadership in Europe and opens an Early Access Program in multiple myeloma
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