Scrip is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Despite Ranbaxy Setback, Indian Cos' Drug Research Stays on Course (India)

This article was originally published in PharmAsia News

Executive Summary

The malaria drug industry faced a major setback following the withdrawal of funding by the Medicines for Malaria Venture (MMV) from an attempt by Ranbaxy Ltd. to develop a new antimalarial treatment. Although Ranbaxy plans to go forward, without funding some are skeptical of the drug's chances. However, two other Indian companies also have promising antimalarial drugs in development. Ipca Laboratories Ltd. leads the pack with four prospects. Two of these molecules are being developed with the support of the Central Drug Research Institute and are currently in preclinical or phase I trials. A third molecule, developed by the Indian Institute of Science, is also in preclinical trials. Ipca's fourth drug in the works is just a new dosage of an older treatment. The fifth drug is being tested by Unimark Pharma Ltd. with the support of the MMV. All five drugs are based on some combination of arteminsinin, a Chinese herb. (Click here for more

You may also be interested in...



Investors Go Beserk For Viking, Putting It Top Of Q1 Winners

The top 10 biggest share price winners and losers in Q1 from Evaluate show the investor frenzy for obesity drugs continues, while companies with governance doubts see shareholders retreat.

EU Consults On What Constitutes Personal & Commercially Confidential Data In Marketing Applications

Based on their experience with dealing with requests for access to documents over the past 12 years, EU regulators have proposed updating their guideline that provides for a harmonized approach to protecting personal data and business secrets in marketing authorization applications.

Industry & Regulators To Align Advice on COVID-19 Vaccine Updates

A multi-stakeholder workshop looked at the data needed to support updates to vaccine composition and the time required by manufacturers to update their vaccines, change their manufacturing processes and prepare approval applications.

Latest Headlines
See All
UsernamePublicRestriction

Register

SC065677

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Thank you for submitting your question. We will respond to you within 2 business days. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel