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No 02 2017

QTE Development

-

May 1, 2017

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Updated: February 17, 2025, 01:49 pm

Published: May 1, 2017

Top stories

Global report – December 9, 2025

Pfizer enters into agreement with YaoPharma

Pfizer has entered into an exclusive global collaboration and license agreement with YaoPharma, a subsidiary of Shanghai Fosun Pharmaceutical for the development, manufacturing and commercialization of YP05002, a small molecule glucagon-like peptide 1 (GLP-1) receptor agonist currently in Phase 1 development for chronic weight management.

MedTech Business – December 9, 2025

CellaVision receives CE marking

CellaVision has announced that its new CellaVision Bone Marrow Aspirate (BMA) Application has received CE marking approval as a Class C product under the European Union In Vitro Diagnostic Regulation (EU IVDR).

Biotech Business – December 9, 2025

Leqembi included in China’s commercial insurance innovative drug list

BioArctic’s partner Eisai has announced that Leqembi (lecanemab), has been included in the “Commercial Insurance Innovative Drug List”, recently introduced by the National Healthcare Security Administration (NHSA) of China.

Pharma Business – December 9, 2025

Xinnate receives FDA IND approval

The US Food and Drug Administration (FDA) has approved the company’s Investigational New Drug (IND) application for TCP-25, a novel topical immunomodulatory peptide being developed for the treatment of Epidermolysis Bullosa (EB).

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Related posts

Global report - December 9, 2025

Pfizer enters into agreement with YaoPharma

Pfizer has entered into an exclusive global collaboration and license agreement with YaoPharma, a subsidiary of Shanghai Fosun Pharmaceutical for the development, manufacturing and commercialization of YP05002, a small molecule glucagon-like peptide 1 (GLP-1) receptor agonist currently in Phase 1 development for chronic weight management.

MedTech Business - December 9, 2025

CellaVision receives CE marking

CellaVision has announced that its new CellaVision Bone Marrow Aspirate (BMA) Application has received CE marking approval as a Class C product under the European Union In Vitro Diagnostic Regulation (EU IVDR).

Biotech Business - December 9, 2025

Leqembi included in China’s commercial insurance innovative drug list

BioArctic’s partner Eisai has announced that Leqembi (lecanemab), has been included in the “Commercial Insurance Innovative Drug List”, recently introduced by the National Healthcare Security Administration (NHSA) of China.

Pharma Business - December 9, 2025

Xinnate receives FDA IND approval

The US Food and Drug Administration (FDA) has approved the company’s Investigational New Drug (IND) application for TCP-25, a novel topical immunomodulatory peptide being developed for the treatment of Epidermolysis Bullosa (EB).

In a new job - December 9, 2025

PharmaRelations appoints new CDO and EVP Denmark

Niels Buch Leander has been appointed new Chief Digital Officer (CDO) and Executive Vice President (EVP) Denmark.

New Market - December 9, 2025

Cinclus Pharma’s linaprazan glurate earns China’s National Reimbursement Listing

Cinclus Pharma Holding's drug linaprazan glurate has been included in China’s 2025 National Reimbursement Drug List (NRDL) for the treatment of gastroesophageal reflux disease (GERD).

Clinical Trials - December 8, 2025

Aurealis Therapeutics announces positive Phase 2 results

The company has announced positive blinded evaluator efficacy results and completion of the Database Lock (DBL) in its DIAMEND Phase 2 clinical trial of AUP-16, the company’s lead asset for the treatment of non-healing neuro-ischemic Diabetic Foot Ulcers (DFUs).

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