Remove clinical cervical-cancer
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Nykode Therapeutics Expands its Clinical Collaboration and Supply Agreement with Roche to Evaluate VB10.16 for Advanced Cervical Cancer

PharmaShots

Shots: The companies expanded their collaboration to evaluate Nykode’s VB10.16, a wholly owned off-the-shelf therapeutic cancer vaccine candidate in the (VB-C-04) trial for patients with advanced cervical cancer in combination with Roche’s atezolizumab. at the time of analysis, and m-PFS (6.3mos.)

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FDA Grants Full Approval to Tivdak for Treating Recurrent or Metastatic Cervical Cancer Patients Experiencing Disease Progression After Chemotherapy

PharmExec

Approval of Tivdak was based on promising results from a Phase III innovaTV 301 clinical trial, which demonstrated a 30% reduction in the risk of death in patients with recurrent or metastatic cervical cancer.

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Merck shares results for Keytruda in cervical cancer treatment

Pharmafile

Merck, known as MSD outside of the US and Canada, has announced positive results from the phase 3 KEYNOTE-A18 trial, which investigates Keytruda in combination with chemoradiotherapy for the treatment of newly diagnosed patients with high-risk locally advanced cervical cancer.

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First immunotherapy recommended for advanced cervical cancer

European Pharmaceutical Review

Pembrolizumab (Keytruda) has been recommended in National Institute for Health and Care Excellence (NICE) final draft guidance for advanced cervical cancer. Clinical trial evidence shows that the treatment helps delay worsening of the disease , compared to standard care.

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SGN-1 by Guangzhou Huajin Pharmaceutical Technology for Cervical Cancer: Likelihood of Approval

Pharmaceutical Technology

SGN-1 is under clinical development by Guangzhou Huajin Pharmaceutical Technology and currently in Phase II for Cervical Cancer.

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Genmab and Pfizer’s TIVDAK sBLA secures full FDA approval

Pharmaceutical Business Review

As per the announcement, the full approval is based on the outcomes of the global, randomised, Phase III innovaTV 301 clinical trial. During the trial, TIVDAK demonstrated a primary endpoint achievement of overall survival (OS) in patients with previously treated recurrent or metastatic cervical cancer, outperforming chemotherapy.

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Volrustomig by AstraZeneca for Cervical Cancer: Likelihood of Approval

Pharmaceutical Technology

Volrustomig is under clinical development by AstraZeneca and currently in Phase III for Cervical Cancer.

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