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You searched for : NMPA  

CanSinoBIO CSO Shares the Latest Results of the Company's Globally Innovative Pneumococcal Vaccine

CanSinoBIO will continue to drive the innovation and development of vaccines with a global vision by enhancing collaboration with international partners, and contributing more to ...
Apr 29

WuXi Biologics launches a new GMP commercial drug product facility

Latest Pharma news updates...
Nov 02

Everest Medicines Announces Approval of Investigational New Drug Application by China NMPA for SPR206

Latest pharma news update...
Sep 27

Innovent and GenFleet announce Exclusive Global License agreement for GFH925 (KRAS G12C Inhibitor)

Latest Pharma News update...
Sep 03

ImmixBio and BeiGene to evaluate combination of IMX-110 and Tislelizumab in solid tumors

Latest Pharma News Update...
Aug 31

Orpathys approved in China for patients with lung cancer and MET gene alterations

This approval follows a priority review designation by the Center for Drug Evaluation of China’s National Medical Products Administration (NMPA) and marks the first ...
Jun 23

Sorrento receives FDA clearance Phase 2 study for Sti-3031 ; Advanced Urothelial Carcinoma

Sorrento intends to combine a variety of its proprietary mAbs in conjunction with the ADNAB technology platform...
Apr 28

Sirnaomics Initiates Phase 2b Study using STP705 for treatment of Squamous Cell Skin Cancer

Surgery is currently the most common treatment option for the treatment of NMSC which often carry significant cutaneous adverse events, risk of scar, infection, bleeding ...
Apr 27

Sirnaomics Initiates Phase 2b Study using STP705 for treatment of Squamous Cell Skin Cancer

Surgery is currently the most common treatment option for the treatment of NMSC which often carry significant cutaneous adverse events, risk of scar, infection, bleeding ...
Apr 27

NMPA Approves Toripalimab in patients with recurrent or metastatic Nasopharyngeal Carcinoma

Approval comes after Failure of at Least Two Lines of Prior Systemic Therapy...
Feb 22

Sirnaomics announces first patient dosed In phase 2a study of STP705

The product candidate has received multiple IND approvals from both the US FDA and Chinese NMPA...
Jan 18

Generex and NuGenerex Immuno-Oncology on last stages of developing li-Key Covid vaccine

The new Complete Vaccine is also suitable for pregnant women and children...
Jan 05

Innovent Biologics announces the NMPA granted new indication approval for BYVASDA

BYVASDA is an anti-vascular endothelial growth factor (VEGF) humanized monoclonal antibody and a bevacizumab biosimilar independently developed by Innovent Biologics...
Dec 28

Arctic Vision obtains the first IND approval for the treatment of UME in China, Suprachoroidal space (SCS) injection potentially brings more benefits to patients

It will be the first clinical trial in China for UME treatment, and also the first one in China to adopt suprachoroidal space (SCS) injection, ...
Dec 26

Innovent Biologics announces NMPA of China granted new indication approvals for SULINNO

Innovent announces NMPA granted new indication approvals for SULINNO (Adalimumab Injection) for the treatment of pediatric plaque psoriasis and non-infectious uveitis ...
Dec 24

Sirnaomics reports positive data from phase 2a study of STP705 for treatment of squamous cell skin cancer

The primary endpoint of this trial was to evaluate patients for complete histological clearance of the tumour cells within the treated isSCC lesion...
Dec 21

Antengene announces acceptance of IND application in China

Antengene announces acceptance of IND application in China for ATG-010 (selinexor) in combination with R-GDP (SR-GDP) for the treatment of rrDLBCL in ...
Dec 07

Lokelma label update approved in China for patients with hyperkalaemia on chronic haemodialysis

The NMPA has approved a dosing label update in China for AstraZeneca’s Lokelma to include patients with hyperkalaemia on chronic haemodialysis....
Nov 25

BioShin enrolls first patient into an Asia-Pacific regional multi-center phase III clinical trial of rimegepant (BHV-3000) for the acute treatment of migraine

BHV3000-310 is a double-blind, randomized trial evaluating the safety and efficacy of rimegepant in the acute treatment of migraine....
Nov 23

Thermo Fisher Scientific partners with Innoforce to establish drug manufacturing facility in China

Joint venture expands global pharma services capacity for drug development and manufacturing ...
Nov 06

Everest Medicines receives approval of CTA by China NMPA for phase 3 registration trial of Trodelvy

This trial will enroll approximately 330 HR+/HER2- mBC patients in Mainland China, Taiwan and South Korea...
Nov 02

Innovent and Eli Lilly announce the NMPA granted marketing approval for HALPRYZA in China

The survival rate is also relatively higher than other tumour types when having appropriate treatment...
Oct 09

SK Biopharmaceuticals start Phase 3 clinical studies for Cenobamate, XCOPRI in Asia

The drug trial will start in Korea and China, Cenobamate Tablets are used for partial-onset seizures in adult...
Sep 14

Junshi Biosciences receives FDA Breakthrough Therapy Designation for Toripalimab

Major breakthrough for treatment of Nasopharyngeal Carcinomar ...
Sep 11

MicroPort CardioFlow Completes Raising New Round of Funds

MicroPort Scientific Corporation completes raising new round of funds for MicroPort CardioFlow Medtech. Corporation....
Apr 17

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