Study of Telotristat (Xermelo) in Combination With Luetetium Lu177 Dotatate (Lutathera) in Well-Differentiated Neuroendocrine Tumors

Status: Discontinued

Phase of Trial: Phase II

Latest Information Update: 29 Jun 2023

Price :

Note:

Adis is an information provider.
Final gross price and currency may vary according to local VAT and billing address.
Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
A link to download a PDF version of the trial profile will be included in your email receipt.

Drugs Lutetium-(177Lu)-oxodotreotide (Primary) ; Telotristat etiprate (Primary)
Indications Neuroendocrine tumours
Focus Therapeutic Use

16 Feb 2023 Status changed from suspended to discontinued.
30 Jun 2022 According to a Novartis media release, company has remediated the issues that led to the temporary, voluntary suspension. These issues did not affect patient safety, and no risk to patients from the doses previously produced at these sites was identified. Company restarted screening and enrollment for clinical trials with Lutathera in the US and Canada.
05 May 2022 According to Novartis media release, status changed to suspended as Novartis is putting a temporary hold on screening and enrollment for Lutathera clinical trials in the US and Canada.

If your organization or you do not have a subscription, try one of the following:

Contacting your organization’s admin about adding this content to your AdisInsight subscription
Buying a PDF version of any individual profile
Request a free trial

If your organization has a subscription, there are several access options, even while working remotely:

Working within your organization’s network
Login with username/password or try to access via your institution
Persisted access using your organization’s identifier stored in your user browser for 90 days

For assistance, contact us at asktheexpert.adisinsight@springer.com