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VV116 Versus PAXLOVID Phase III Registrational Trial for Early Treatment of Mild to Moderate COVID-19 in High Risk Patients Reaches Primary Endpoint

Press release content from Globe Newswire. The AP news staff was not involved in its creation.

United statesSan franciscoJunshi bioscienceJunshi biosciencesZhi liActa pharmacologica sinicaIr teamCentral asian centerChinese academy of sciencesXinjiang technical institute of physicsVigonvita life sciences co ltdPr teamInstitute of microbiology the chinese academyShanghai institute of materia medicaWuhan institute of virologyShanghai junshi biosciences co ltd

Investegate |Junshi Biosciences Announcements | Junshi Biosciences: VV116 Versus PAXLOVID Phase III Registrational Trial for Early Treatment of Mild to Moderate COVID-19 in High Risk Patients Reaches Primary Endpoint

Investegate announcements from Junshi Biosciences, VV116 Versus PAXLOVID Phase III Registrational Trial for Early Treatment of Mild to Moderate COVID-19 in High Risk Patients Reaches Primary Endpoint

United statesSan franciscoJunshi bioscienceJunshi biosciencesZhi liActa pharmacologica sinicaIr teamCentral asian centerChinese academy of sciencesXinjiang technical institute of physicsVigonvita life sciences co ltdPr teamInstitute of microbiology the chinese academyShanghai institute of materia medicaWuhan institute of virologyShanghai junshi biosciences co ltd

VV116 Versus PAXLOVID Phase III Registrational Trial for

the study reached its primary endpoint(VV116 was statistically superior) and secondary efficacy endpoint VV116 has a favorable safety profile and.

United statesSan franciscoJunshi bioscienceJunshi biosciencesZhi liActa pharmacologica sinicaIr teamCentral asian centerChinese academy of sciencesXinjiang technical institute of physicsVigonvita life sciences co ltdPr teamInstitute of microbiology the chinese academyShanghai institute of materia medicaWuhan institute of virologyShanghai junshi biosciences co ltd

VV116 Versus PAXLOVID Phase III Registrational Trial for Early Treatment of Mild to Moderate COVID-19 in High Risk Patients Reaches Primary Endpoint | Comunicados | Edición USA

VV116 Versus PAXLOVID Phase III Registrational Trial for Early Treatment of Mild to Moderate COVID-19 in High Risk Patients Reaches Primary Endpoint | Comunicados | Edición USA
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United statesSan franciscoJunshi bioscienceJunshi biosciencesZhi liActa pharmacologica sinicaIr teamCentral asian centerChinese academy of sciencesXinjiang technical institute of physicsVigonvita life sciences co ltdPr teamInstitute of microbiology the chinese academyShanghai institute of materia medicaWuhan institute of virologyShanghai junshi biosciences co ltd

Junshi Biosciences Receives NMPA Approval of sNDA for Toripalimab in Combination with Paclitaxel and Cisplatin in First-Line Treatment of Advanced or Distant Metastatic Esophageal Squamous Cell Carcinoma – Indonesia Tribune

Junshi Biosciences Receives NMPA Approval of sNDA for Toripalimab in Combination with Paclitaxel and Cisplatin in First-Line Treatment of Advanced or Distant Metastatic Esophageal Squamous Cell Carcinoma – Indonesia Tribune
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United statesSan franciscoRuihua xuPatricia keeganJunshi bioscienceJunshi biosciencesZhi liJianjun zouGlobal researchIr teamSun yat sen university cancer centerNational reimbursement drug listChina national medical products administrationPr teamInstitute of microbiology the chinese academyShanghai junshi biosciences co ltd