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Replimune Provides Data Update from its RP1 (vusolimogene oderparepvec) and RP2 Programs and Announces Plans to Expand the Development of RP2/3 Beyond Phase 1

High rate of complete responses in RP1 skin cancer cohorts underscore the potential for profound patient benefit and supports the ongoing registration directed development programs RP2 data confirms the signal with RP1 in anti-PD1 failed melanoma, uveal melanoma and in treating patients whose cancer has metastasized to the liver Announces plans to initiate broad Phase 2 development of RP2 and/or RP3 in tumor types that commonly metastasize to the liver Virtual investor event to be held at 8:00 a
Tumor Types Clinical Trial Liver Metastases Melanoma Patients Primary Endpoint Complete Response
Source: yahoo.com

CStone Announces the First - in - Class Registrational Clinical Trial of Sugemalimab Met its Primary Endpoint in Stage III NSCLC and Plans

... and commercializing innovative immuno - oncology therapies and precision medicines, today ... It has also been granted Breakthrough Therapy Designation by ...
National Medical Products Administration Registrational Clinical Trial Sugemalimab Met Primary Endpoint Breakthrough Therapy Designation ப்ரைமரீ இறுதிப்புள்ளி
Source: zazoom.it

Valneva : and Pfizer Announce Initiation of Phase 2 Study for Lyme Disease Vaccine Candidate

Pfizer Forward-Looking Statements The information contained in this release is as of March 8, 2021. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.  This release contains forward-looking information about a Lyme disease vaccine candidate, VLA15, and a collaboration between Pfizer and Valneva for VLA15, including their potential benefits and a potential phase 3 start, that involves su...
United States New York Kathrin Jansen Bryan Dunn Juan Carlos Jaramillo Jerica Pitts

Valneva and Pfizer Announce Initiation of Phase 2 Study for Lyme Disease Vaccine Candidate

Press release content from Globe Newswire. The AP news staff was not involved in its creation. Valneva and Pfizer Announce Initiation of Phase 2 Study for Lyme Disease Vaccine Candidate VALNEVAMarch 8, 2021 GMT The Phase 2 study will include both adult and pediatric subjects with an aim to support acceleration of the vaccine candidate’s pediatric program   VLA15 will be  tested at two different schedules (Month 0-2-6 or Month 0-6) receiving the selected dose of 180µg VLA15 is the only Lyme...
United States New York Kathrin Jansen Bryan Dunn Juan Carlos Jaramillo Jerica Pitts
Source: apnews.com

CTA Matches Invasive Angiography for Stratification of NSTE ACS Risk

February 23, 2021 Coronary computed tomographic angiography (CTA) may be as good as invasive coronary angiography (ICA) at predicting the long-term risk of adverse events in patients with non-ST-segment elevation acute coronary syndromes, according to a subanalysis of the VERDICT trial. “The key thing is that its pretty much equivalent whether you do an ICA or you do a CT to define the likelihood of events after the MI,” lead author Klaus F. Kofoed, MD, DmSc (University of Copenhagen, Denma...
United States United Kingdom City Of Michellec Williams Klausf Kofoed Udo Hoffmann
Source: tctmd.com

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Aprea Therapeutics Announces Results of Primary Endpoint from Phase 3 Trial of Eprenetapopt in TP53 Mutant Myelodysplastic Syndromes (MDS) | Small Molecules

Hits: 1013 The trial failed to meet its primary endpoint of complete remission (CR) rate CR rate was 53% higher in eprenetapopt with AZA arm compared to AZA alone, but did not reach statistical significance BOSTON, MA, USA I December 28, 2020 I Aprea Therapeutics, Inc. (Nasdaq: APRE), a biopharmaceutical company focused on developing and commercializing novel cancer therapeutics that reactivate the mutant tumor suppressor protein, p53, today announced results of the primary data cut from it...
United States International Working Group I Aprea Therapeutics Inc European Commission European Medicines Agency Aprea Therapeutics Inc

KITE'S TECARTUS®▼ (AUTOLOGOUS ANTI-CD19-TRANSDUCED CD3+ CELLS) GRANTED CONDITIONAL MARKETING AUTHORISATION FOR THE TREATMENT OF ADULT PATIENTS WITH RELAPSED OR REFRACTORY MANTLE CELL LYMPHOMA AFTER TWO OR MORE LINES OF SYSTEMIC THERAPY INCLUDING A BRUTON'S TYROSINE KINASE (BTK) INHIBITOR

utologous anti CD19 transduced CD3+ cells Granted Conditional European Marketing Authorisation for Relapsed and Refractory Mantle Cell Lymphoma --   London, UK – 16 December 2020 – Kite, a Gilead Company, today announced that the European Commission has granted conditional marketing authorisation for its autologous anti CD19 transduced CD3+ cells, a chimeric antigen receptor (CAR) T cell therapy, as a treatment for adult patients with relapsed or refractory mantle cell lymphoma after two ...
United Kingdom City Of Ken Takeshita Anthony Nolan Antonio Pagliuca Ropinder Gill

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