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Immunomodulator
1 for Non-Small Cell Lung Cancer (FORTIS-C Trial)
Phase 3
Waitlist Available
Research Sponsored by Agennix
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at the time of final analysis
Awards & highlights
FORTIS-C Trial Summary
The purpose of the study is to determine whether the combination of talactoferrin, carboplatin and paclitaxel improves progression free survival and overall survival in patients with non-small cell lung cancer compared to the combination of paclitaxel and carboplatin alone
Eligible Conditions
- Non-Small Cell Lung Cancer
FORTIS-C Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ after the occurence of the required number of events
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~after the occurence of the required number of events
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Overall Survival
Progression free survival
Secondary outcome measures
Objective response and disease stabilization rate
Safety and tolerability
FORTIS-C Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: 1Experimental Treatment1 Intervention
Talactoferrin, Carboplatin, Paclitaxel
Group II: 2Placebo Group1 Intervention
Placebo, Carboplatin, Paclitaxel
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Talactoferrin alfa
Not yet FDA approved
Find a Location
Who is running the clinical trial?
AgennixLead Sponsor
19 Previous Clinical Trials
3,039 Total Patients Enrolled
Frequently Asked Questions
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