Molecular Profiles Chosen to Develop Topical and Oral Formulations of Telormedix's Psoriasis Product - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Molecular Profiles Chosen to Develop Topical and Oral Formulations of Telormedix's Psoriasis Product


Molecular Profiles, a Nottingham-based CDMO, has secured a major pan-European formulation project, in which the company will be responsible for developing a topical and an oral formulation for Telormedix’s psoriasis products, TMX-302. The international research project, known as PAT (Psoriasis Anti-inflammatory Treatment), will also involve other consortium partners Biopta, Midatech Biogune and the University Hospital Zurich.

Telormedix, a clinical stage biopharmaceutical company, has raised funding from the European Eurostars Programme to coordinate the TMX-302 project, which will use Midatech’s glycan-coated gold nanoparticles formulated using Molecular Profiles’ expertise. 
Johanna Holldack, CEO at Telormedix, said in a press statement that “the team at Molecular Profiles will play a key role in developing new oral and topical formulations of TMX-302, both of which are viewed as practicable administration options for the treatment of psoriasis.”



Just a few weeks ago, Molecular Profiles announced the official opening of its new clinical manufacturing facility following a successful inspection from the Medical and Healthcare products Regulatory Agency (MHRA). Molecular Profiles was also recently acquired by Columbia Laboratories, a Boston-based drug development company.

“We are pleased to have been chosen as the formulation development partner for this high-profile, multi-partner project,” said Nikin Patel, CEO of Molecular Profiles in a press statement. “Our team is ready to apply our technologies to deliver a robust topical and oral formulation.”
 The company’s new facility can handle a range of dosage forms such as solids, liquids, semi-solids and inhaled products and has the capacity to manufacture controlled drugs and highly potent compounds up to OEB 4 level with batch scale of up to 30kg.

Source: Molecular Profiles

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
33%
Breakthrough designations
11%
Protecting the supply chain
39%
Expedited reviews of drug submissions
11%
More stakeholder involvement
6%
View Results
Jim Miller Outsourcing Outlook Jim Miller Health Systems Raise the Bar on Reimbursing New Drugs
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerThe Mainstreaming of Continuous Flow API Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler Industry Seeks Clearer Standards for Track and Trace
Siegfried Schmitt Ask the Expert Siegfried SchmittData Integrity
Sandoz Wins Biosimilar Filing Race
NIH Translational Research Partnership Yields Promising Therapy
Clusters set to benefit from improved funding climate but IP rights are even more critical
Supplier Audit Program Marks Progress
FDA, Drug Companies Struggle with Compassionate Use Requests

Click here