AMRI Stock Tumbles After Announcing B-MS Trial Ends

By Zachary Brennan

- Last updated on GMT

AMRI Stock Tumbles After Announcing B-MS Trial Ends

Related tags Food and drug administration Bristol-myers squibb Amri

Albany Molecular Research's (AMRI) stock fell more than 10% on Monday after announcing in an SEC filing that it was informed by its partner Bristol-Myers Squibb that it would terminate the development of an investigational depression drug.

But the decision to cease the drug’s development, which was in Phase II of clinical development, is expected to “have no impact on AMRI’s financial guidance or forecasts, including, the company’s financial guidance for the third quarter and full year 2013​,” AMRI said.

The partnership between AMRI and BMS began in 2005 and has been a source of revenue for AMRI in the past due to payments for research and milestones reached on some compounds.

The drug in question was a triple reuptake inhibitor in development for treatment-resistant depression.

The announcement of the trial’s end comes as the company recently received a Form 483 at its Burlington, Massachusetts, plant​ after the US FDA re-inspected it.  

Despite these setbacks, AMRI CEO Thomas D’Ambra said last week in an earnings call​ that the company still expects to be profitable by the end of the year.

Related news

Show more

Related products

show more

Automated metadata management in clinical trials

Automated metadata management in clinical trials

Content provided by Formedix | 01-Aug-2023 | White Paper

When it comes to efficient clinical study build, content is king. Most importantly: metadata content. In this blog, we explore the role of metadata in...

Small Molecule development – getting it right

Small Molecule development – getting it right

Content provided by Lonza Small Molecules | 20-Jun-2023 | Insight Guide

Small Molecule drug development is something more and more ambitious emerging pharmaceutical companies are taking on from end to end. But this path can...

Validate clinical study data with Formedix CORE

Validate clinical study data with Formedix CORE

Content provided by Formedix | 19-Jun-2023 | White Paper

In April 2023 at the CDISC Europe Interchange, we launched Formedix CORE, the first free-to-use, downloadable application encompassing the CDISC Open Rules...

The Right CDMO Can Unlock Faster Drug Development

The Right CDMO Can Unlock Faster Drug Development

Content provided by Lonza Small Molecules | 15-May-2023 | Interview

Drug development presents biotech companies with ever-changing challenges. Enabling a faster end-to-end process requires seamless flexibility and extensive...

Related suppliers

Follow us

Products

View more

Webinars