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Health Source (600380): Performance is in line with expectations, and Tubuu is expected to accelerate its volume quarterly
Guide to this report: The collection of zoxa and budesonide caused respiratory pressure for 24 years. Tobramycin is expected to accelerate quarterly release, and salmetroticasone is expected to be approved for marketing in 24Q2, which is expected to drive positive respiratory growth and maintain an “increase in maintenance” rating. invests
Health Source (600380): 1Q24 results are in line with expectations, TG-1000 reached the main phase III clinical endpoint
1Q24 results are in line with our expectations Health Yuan announced results for the first quarter of 2024: operating income of 4.34 billion yuan, down 4.81% year on year; net profit to mother of 440 million yuan (corresponding to basic earnings per share of 0.24 million yuan
Express News | Health Source: The company's injectable cetrorelix acetate was approved by the US FDA
Health Yuan (600380.SH) announced first-quarter results, net profit of 440 million yuan, a year-on-year decrease of 4.96%
According to the Zhitong Finance App, Health Yuan (600380.SH) disclosed its report for the first quarter of 2024. During the reporting period, the company achieved revenue of 4.34 billion yuan, a year-on-year decrease of 4.81%; net profit to mother was 440 million yuan, a year-on-year decrease of 4.96%; after deducting non-net profit of 428 million yuan, a year-on-year decrease of 4.26%. Basic earnings per share were $0.2357.
Joincare Pharma Says Flu Drug Phase 3 Trial Attains Primary Endpoint
Joincare Pharmaceutical Group (SHA:600380) said its phase 3 trial for TG-1000 capsules as a treatment for influenza A and B reached the primary research endpoint, according to a Thursday filing with t
Health Source (600380.SH): TG-1000 capsule phase III clinical trial reached the main end
Gelonghui, April 17 | Health Source (600380.SH) announced that recently, the company's innovative drug product TG-1000 capsules for use in a multi-center phase III clinical trial (referred to as this study) with no complications in acute influenza A and B infections aged 12 and above (referred to as this study) reached the end of the main study. The company will communicate with the Drug Evaluation Center (CDE) of the China Drug Administration about the marketing application of TG-1000 capsules to treat influenza in the near future to advance the marketing process of TG-1000 capsules.
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