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Humanwell Healthcare Unit Gets China Clinical Trial Approval for Seizure Treatment
Humanwell Healthcare Subsidiary Gets Approval for Pain Relief Clinical Trials
Humanwell Healthcare (600079.SH): RFUS-301 injection has received the approval notice for clinical drug trials.
Gelonghui, February 27 | Humanwell Healthcare (600079.SH) announced that its holding subsidiary, Yichang Humanwell Pharmaceutical Co., Ltd., recently received the clinical trial approval notice for the RFUS-301 injection issued by the National Medical Products Administration. The RFUS-301 injection is a modified postoperative analgesic developed by Yichang Humanwell. Currently, there are no similar products on the domestic market. So far, Yichang Humanwell has accumulated an investment of about 10 million yuan in research and development for this project.
Humanwell Healthcare Obtains Registration for Pain Management Drug; Shares Up 3%
Humanwell Healthcare (600079.SH): The hydrochloride spray has obtained a pharmaceutical registration certificate.
On February 26, Gelonghui reported that Humanwell Healthcare (600079.SH) announced that its holding subsidiary, Yichang Humanwell Pharmaceutical Co., Ltd. (referred to as 'Yichang Humanwell', in which the company holds 80% of the shares), recently received the 'Pharmaceutical Registration Certificate' approved and issued by the National Medical Products Administration for the hydrochloride of Tapentadol tablets. Hydrochloride of Tapentadol tablets is used for treating acute pain in adult patients who require opioid medication and for whom alternative therapy does not adequately relieve.
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