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NCT01673646 · MORE INFO

Limitations, agreements, and source contact

Efficacy and Safety of Pasireotide LAR (Long-acting Release) in Japanese Patients With Acromegaly or Pituitary Gigantism · Source last updated 2019-09-16

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

certain Agreement
other Details
The terms and conditions of Novartis' agreements with its investigators may vary. However, Novartis does not prohibit any investigator from publishing. Any publications from a single-site are postponed until the publication of the pooled data (i.e., data from all sites) in the clinical trial or disclosure of trial results in their entirety.
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
After the first 3 months, pasireotide LAR dose could be increased for efficacy or decreased for safety at any time during the study.
point Of Contact
email
novartis.email@novartis.com
organization
Novartis Pharmaceuticals
phone
862-778-8300
title
Clinical Disclosure Office
Complete source fields
certain Agreement
other Details
The terms and conditions of Novartis' agreements with its investigators may vary. However, Novartis does not prohibit any investigator from publishing. Any publications from a single-site are postponed until the publication of the pooled data (i.e., data from all sites) in the clinical trial or disclosure of trial results in their entirety.
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
After the first 3 months, pasireotide LAR dose could be increased for efficacy or decreased for safety at any time during the study.
point Of Contact
email
novartis.email@novartis.com
organization
Novartis Pharmaceuticals
phone
862-778-8300
title
Clinical Disclosure Office

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Preserved source evidence · Not medical advice