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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02057380
Other study ID # 7487-CL-0209
Secondary ID 2013-004076-34
Status Completed
Phase Phase 2
First received
Last updated
Start date April 16, 2014
Est. completion date December 21, 2016

Study information

Verified date August 2018
Source Astellas Pharma Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to provide access to continued treatment for subjects who participated in other Astellas sponsored trials and for whom the investigator feels the subject may benefit from continued treatment.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date December 21, 2016
Est. primary completion date October 14, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subject must currently be participating in an Astellas sponsored linsitinib trial that has ended with respect to the overall study analysis.

- Subject must not have met criteria for discontinuation or have progressed on the current linsitinib study in which they are participating.

- Subject must be deriving benefit from continued treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
linsitinib
oral
erlotinib
oral
paclitaxel
Intravenous (IV) infusion
Bortezomib
Subcutaneous or IV
Dexamethasone
IV, Oral

Locations

Country Name City State
Brazil Site BR55005 Porto Alegre Rio Grande Do Sul
Czechia Site CZ42001 Ostrava-Poruba
Germany Site DE49002 Berlin
Germany Site DE49001 Wuerzburg
Poland Site PL48001 Szczecin Zachodniopomorskie
Singapore Site SG65002 Singapore
Thailand Site TH66003 Khon Kaen
United States Site US10008 Ann Arbor Michigan
United States Site US10002 Baltimore Maryland
United States Site US10004 La Jolla California
United States Site US10001 Oklahoma City Oklahoma
United States Site US10006 Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
Astellas Pharma Global Development, Inc.

Countries where clinical trial is conducted

United States,  Brazil,  Czechia,  Germany,  Poland,  Singapore,  Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of subjects with adverse events 24 months
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