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Unveiling Cellular Recycling: How Nutrient-Starved Cells Adapt to Stressful Conditions

The findings revealed a remarkable cellular response wherein nutrient-starved cells reroute ER exit sites to lysosomes, organelles responsible for degrading and recycling cellular material....
Apr 16

1 Press Note Sanofi India Limited and Emcure Pharmaceuticals announce exclusive distribution partnership to broaden reach of Sanofi’s Cardiovascular brands

Sanofi continues to give fresh impetus to its business in the Country with an accelerated growth plan - ‘India for India’, across its pharmaceuticals, specialty, consumer ...
Mar 13

Telangana Police launched India’s First Law Enforcement CISO Council

It is termed as a Beacon of Cybersecurity in Telangana. DGP Anjani Kumar, Principal Secretary Jayesh Ranjan unveiled amidst the presence of Commissioner of Cyberabad, ...
Oct 23

Jagananna Arogya Suraksha Scheme: A Lifeline for the Poor in Andhra Pradesh

This survey goes beyond identifying common illnesses; it also focuses on chronic health conditions and nutritional needs of pregnant women, new mothers, underweight individuals, and ...
Sep 08

World Rare Disease Day: End Stigma Against Rare Diseases.

Celebrating World Rare Disease Day will create awareness and encourage patients to seek medical help on time to manage their condition....
Feb 28

Helex can now cure inherited blindness and cancer by gene editing

Gene editing is a technique for making specific changes to a cell's or organism's DNA. It can be used to insert, remove, or ...
Aug 30

Phablecare gains $25 million in its Series B round

Chronic disease management startup Phablecare has gained $25 million (Rs 187 crore) in its Series B funding round led by Kalaari Capital. ...
Apr 12

Phablecare acquires Fused Training

India’s largest chronic disease management venture Phablecare has acquired a type 1 diabetes combating startup Fused Training....
Apr 02

Sio Gene Therapies recieves FDA Fast track designation for AXO-AAV-GM2 Gene Therapy in patients Gangliosidosis

Latest pharma news update...
Nov 03

Takeda to commercialize Hunter Syndrome Therapy through collaboration with JCR Pharmaceuticals

Latest pharma news update...
Oct 04

Dr Vikas gives insights into lung cancer which can be prevented

Stay tuned and watch the entire episode of the lung cancer awareness series with Dr. Vikas knows the real cause of lung cancer which is ...
Sep 01

GC Pharma and Tottori University collaborates for development of GM1 Gangliosidosis Chaperone Therapy

Latest pharma news update...
Aug 03

FDA approves nasal antihistamine for nonprescription use

Seasonal allergies affect millions causing nasal congestion, runny nose and sneezing. Approval of Asteopro (Azelastine Hydrochloride nasal spray 0.15%) can help many patients with ...
Jun 18

Forge Biologics receives USFDA fast track, orphan drug, and rare pediatric disease designations

Forge Biologics receives FDA fast track, orphan drug, and rare pediatric disease designations for FBX-101 gene therapy for patients with krabbe disease ...
Feb 17

Sosei Heptares collaborates with GlaxoSmithKline targeting immune disorders of the digestive system

GSK licenses global rights to a portfolio of GPR35 agonists designed by Sosei Heptares using its StaR technology and structure-based drug design platform...
Dec 22

Polaryx Therapeutics Receives Both Rare Pediatric Disease and Orphan Drug Designations for the Treatment of Niemann Pick Disease Types A and B With PLX-300

Polaryx Therapeutics, today announced that it has received from the U.S. Food and Drug Administration (FDA) both Rare Pediatric Disease and Orphan Drug Designations ...
Dec 18

Biogen Files New Drug Application for Aducanumab in Japan

Today, Biogen and Eisai, Co., Ltd. announced that Biogen has submitted a Japanese New Drug Application (J-NDA) to the Ministry of Health, Labor and ...
Dec 10

Polaryx Therapeutics receives both rare pediatric disease and orphan drug designations from US FDA

Polaryx Therapeutics has received from the US FDA both Rare Pediatric Disease and Orphan Drug designations for the treatment of GM2 gangliosidosis with PLX-300...
Nov 25

FDA grants priority review for avalglucosidase alfa, a potential new therapy for Pompe disease.

The U.S. Food and Drug Administration (FDA) has accepted for priority review the Biologics License Application (BLA) for avalglucosidase alfa for long-term enzyme ...
Nov 20

Common cold antibodies hold clues to COVID-19 behavior; lung scans speed COVID-19 diagnosis in stroke patients

Common cold antibodies yield clues to COVID-19 behavior....
Nov 07

FDA advisory panel not convinced of experimental Alzheimer's drug's effectiveness

Public Citizen's Health Research Group said that the FDA should not approve aducanumab for treatment of Alzheimer's disease due to lack of evidence ...
Nov 07

Prevail Therapeutics receives U.S. FDA fast track designation for PR001

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Oct 30

Passage Bio’s PBGM01 receives Orphan Drug Designation from EMA for treatment of GM1 Gangliosidosis

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Oct 27

Bristol Myers Squibb to acquire MyoKardia for $13.1 billion in cash

The acquisition of MyoKardia further strengthens Bristol Myers Squibb's portfolio, pipeline and scientific capabilities...
Oct 12

EMA accepts regulatory submission for avalglucosidase alfa for Pompe disease

Avalglucosidase alfa is an investigational enzyme replacement therapy, which, if approved, would offer a potential new standard of care for patients with Pompe disease...
Oct 02

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