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

Strike two for Lilly's novel schizophrenia drug

This article was originally published in Scrip

Executive Summary

The large Phase II study (HBBM) on its pipeline schizophrenia drug LY2140023 has yielded the worst possible outcome for Eli Lilly. The Lilly drug trial could not be separated from placebo at either one of two doses, and therefore missed its primary efficacy endpoint. Not only that, the active comparator in the trial, risperidone, a generic drug since 2003, did demonstrate efficacy at a statistically significant level. The latest failure - coupled with LY2140023's already uncertain efficacy profile - casts serious uncertainty over whether the drug will reach the market.

You may also be interested in...



Will J&J TRANSFORM Esketamine Into A Viable Depression Treatment?

In early 2018 Johnson & Johnson is expecting to announce the first data from its long-awaited pivotal clinical trial program for esketamine in treatment-resistant depression; a successful result will open a lucrative commercial opportunity for J&J and give the wider depression market a new direction for growth.

If Alkermes Antidepressant Can Get Past FDA, The Market Might Be There

Alkermes’s announcement of positive findings in the FORWARD-5 trial of its treatment-resistant depression drug ALKS 5461 came as a surprise, given the past two Phase III trials disappointed, but if it can gain approval, the buprenorphine/samidorphan product could meet an unmet need.

Kyprolis ENDEAVOR data signal a changing of the guard for multiple myeloma treatment

Amgen revealed more data from the ENDEAVOR study that further demonstrate Kyprolis's (carfilzomib; Amgen/Ono Pharmaceutical) superiority to Velcade (bortezomib; Takeda/Johnson & Johnson) as a second-line treatment for relapsed multiple myeloma.

Topics

Related Companies

Latest Headlines
See All
UsernamePublicRestriction

Register

SC018100

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