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Glaucoma - lerdelimumab (CAT-152) [ID383]

Status: Suspended
Expected date of issue: TBC
Referral date: June 2004
Process: STA
Topic area:
  • Eye
  • Therapeutic procedures
 

NICE project team

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Provisional schedule

Closing date for invited submissions / evidence submission: TBC
1st appraisal committee meeting: 01 January 2100
2nd appraisal committee meeting TBC
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Consultees and commentators

To be confirmed

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Project history

Date Update
25 August 2006 This topic was transferred to the Single technology appraisal (STA) process as part of the Institute's 12th wave work programme.

14 September 2006

As you may be aware, the Department of Health and the Welsh Assembly Government asked the Institute to conduct an appraisal of lerdelimumab for glaucoma, and to provide guidance on its use to the NHS in England and Wales.

Following receipt of trial data, the manufacturer of lerdelimumab has advised us that they have not applied for regulatory approval in relation to this product. The Institute has therefore decided to remove this appraisal from its work programme.

As this topic has been referred to the Institute we will continue to monitor any development and will update interested parties if the situation changes. If you have any comments or concerns please do not hesitate to contact the Project Manager for this appraisal, Cathryn Fuller ( 020 7067 5896 or email: cathryn.fuller@nice.org.uk).

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Key documents

This page was last updated: 28 February 2012

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Selected, reliable information for health and social care in one place

Accessibility | Cymraeg | Freedom of information | Vision Impaired | Contact Us | Glossary | Data protection | Copyright | Disclaimer | Terms and conditions

Copyright 2014 National Institute for Health and Care Excellence. All rights reserved.

Accessibility | Cymraeg | Freedom of information | Vision Impaired | Contact Us | Glossary | Data protection | Copyright | Disclaimer | Terms and conditions

Copyright 2014 National Institute for Health and Care Excellence. All rights reserved.