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Curis Reports Fourth Quarter and Year-End 2020 Financial Results


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LEXINGTON, Mass., March 16, 2021 /PRNewswire/  Curis, Inc. (NASDAQ: CRIS), a biotechnology company focused on the development of innovative therapeutics for the treatment of cancer, today reported its financial results for the fourth quarter and year ended December 31, 2020.
2020 was a transformative year for Curis, as we made significant progress in our mission to develop the next generation of targeted cancer therapies that meaningfully improve and extend the lives of patients. Despite the difficulties and uncertainty brought about by the ongoing coronavirus pandemic, we significantly advanced and expanded each program in our clinical pipeline, headlined by the very encouraging data from our Phase 1 trials of lead asset, CA-4948, presented in December in conjunction with ASH, said James Dentzer, President and Chief Executive Officer of Curis. We look forward to providing additional updates on our IRAK4 program throughout the ....

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Dynavax Announces European Commission Marketing Authorization for HEPLISAV B, a 2 Dose Adult Hepatitis B Adjuvanted Vaccine


Dynavax Announces European Commission Marketing Authorization for HEPLISAV B, a 2 Dose Adult Hepatitis B Adjuvanted Vaccine
Approval based on safety and immunogenicity results from three Phase 3 clinical trials
Statistically significantly higher and faster rates of protection and similar safety compared to Engerix-B in all 3 trials
HEPLISAV B is the only 2-dose adult hepatitis B vaccine offering protection in just 1 month
EMERYVILLE, Calif., Feb. 19, 2021 /PRNewswire/ Dynavax Technologies Corporation (Nasdaq: DVAX), a biopharmaceutical company focused on developing and commercializing novel vaccines, today announced that the European Commission (EC) has granted Marketing Authorization for HEPLISAV B (Hepatitis B Vaccine (Recombinant), Adjuvanted) for the active immunization against hepatitis B virus infection (HBV) caused by all known subtypes of hepatitis B virus in adults 18 years of age and older. The approval was issued following the European Medicine ....

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