Drugs / SYS6006

Trials 7

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT05354063 Jun → Sep 2022 COVID-19 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Unknown No outcome recorded
Phase 1 NCT05354089 Apr → Jul 2022 Orthocoronavirinae infectious disease CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Unknown No outcome recorded
Phase 1/21 trial
Phase 1/2 NCT07622225 May 2026 → Dec 2028 expected neoplasm CSPC Megalith Biopharmaceutical Co.,Ltd. Not yet recruiting No outcome recorded
Phase 21 trial
Phase 2 NCT05439824 Jun 2022 → Jan 2023 COVID-19 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Unknown No outcome recorded
Phase 42 trials
Phase 4 NCT07834073 May 2023 → Feb 2024 COVID-19 Jiangsu Province Centers for Disease Control and Prevention Completed No outcome recorded
Phase 4 NCT05855408 May 2023 → May 2024 COVID-19 Jiangsu Province Centers for Disease Control and Prevention Unknown No outcome recorded
Phase not applicable1 trial
— NCT05492643 Aug 2022 → Feb 2023 COVID-19 Zhongnan Hospital Unknown No outcome recorded

News releases announcing trial results or a regulatory action · 6

DateIssuerRelease
2023-12-01 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - BIVALENT COVID-19 mRNA VACCINE (SYS6006.32) INCLUDED FOR EMERGENCY USE IN CHINA irasia.com ↗
2023-10-30 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - BIVALENT COVID-19 mRNA VACCINE (SYS6006.32) OBTAINS CLINICAL TRIAL APPROVAL irasia.com ↗
The board of directors (the “Board”) of CSPC Pharmaceutical Group Limited (the “Company”, together with its subsidiaries, the “Group”) is pleased to announce that the bivalent COVID-19 mRNA vaccine (XBB.1.5/BQ.1 variants) (SYS6006.32) (the “Product”) developed by the Group has obtained clinical trial approval granted by the National Medical Products Administration of the People’s Republic of China.
2023-03-22 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - SARS-CoV-2 mRNA VACCINE (SYS6006) INCLUDED FOR EMERGENCY USE IN CHINA irasia.com ↗
SARS-CoV-2 mRNA VACCINE(SYS6006) INCLUDED FOR EMERGENCY USE IN CHINA
2022-08-23 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Results VOLUNTARY ANNOUNCEMENT - UPDATE ON THE CLINICAL STUDY PROGRESS OF SARS-CoV-2 mRNA VACCINE (SYS6006) irasia.com ↗
The study started enrollment on 27 April 2022 at Shulan (Hangzhou) Hospital, Zhejiang Province, and currently the safety observation as well as immunogenicity evaluation have been completed for all subjects 30 days after the second dose of vaccination.
2022-08-23 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Results VOLUNTARY ANNOUNCEMENT - COMPLETION OF A CLINICAL STUDY OF HETEROLOGOUS BOOSTER IMMUNIZATION OF SARS-CoV-2 mRNA VACCINE (SYS6006) irasia.com ↗
The Company is pleased to announce that a clinical study of heterologous booster immunization (the “Study”) of the SARS-CoV-2 mRNA vaccine (SYS6006) (the “ Product”) developed by the Group was completed, with the expectations for safety and immunogenicity met.
2022-04-03 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - COVID-19 mRNA VACCINE "SYS6006" OBTAINS CLINICAL TRIAL APPROVAL irasia.com ↗
The board of directors (the “Board”) of CSPC Pharmaceutical Group Limited (the “Company”, together with its subsidiaries, the “Group”) announces that the COVID-19 mRNA vaccine “SYS6006” (the “Product”) developed by the Group has obtained approval granted by the National Medical Products Administration of the People’s Republic of China to conduct clinical trials in China.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as SYS6006 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07834073 ↗
6

NCT05855408 ↗

NCT05354063 ↗

NCT05354089 ↗

NCT07622225 ↗

NCT05492643 ↗

NCT05439824 ↗

Modality Messenger RNA (mRNA) “SARS-CoV-2 mRNA Vaccine (SYS6006)” NCT05354063 ↗
Route Intramuscular “20 μg dose of SYS6006 vaccine IM on day 0 and day 21.” NCT05354063 ↗