NCT02090127

Brief Summary

Protocol to Allow Continued Access of Ficlatuzumab to P05538 Patient

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 14, 2014

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 18, 2014

Completed
Last Updated

July 29, 2015

Status Verified

July 1, 2015

First QC Date

March 14, 2014

Last Update Submit

July 27, 2015

Conditions

Interventions

humanized anti-hepatocyte growth factor (HGF) monoclonal antibody IV administration at 16.5mg/kg every 2 weeks with a ±2 day window around dosing dates, as long as subject is deriving clinical benefit as determined by the Investigator

Also known as: AV-299, SCH 900105

Eligibility Criteria

Age18 Years+
Sexfemale
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Per original P05538 protocol

You may not qualify if:

  • Per original P05538 protocol

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

START

San Antonio, Texas, 78229, United States

Location

Related Links

MeSH Terms

Interventions

ficlatuzumab

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 14, 2014

First Posted

March 18, 2014

Last Updated

July 29, 2015

Record last verified: 2015-07

Locations