A Global Study to Assess the Effects of MEDI4736 Following Concurrent Chemoradiation in Patients With Stage III Unresectable Non-Small Cell Lung Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Lung Cancer, Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 127 |
Updated: | 4/4/2019 |
Start Date: | May 7, 2014 |
End Date: | July 9, 2019 |
A Phase III, Randomised, Double-blind, Placebo-controlled, Multi-centre, International Study of MEDI4736 as Sequential Therapy in Patients With Locally Advanced, Unresectable Non-Small Cell Lung Cancer (Stage III) Who Have Not Progressed Following Definitive, Platinum-based, Concurrent Chemoradiation Therapy (PACIFIC)
A Global Study to Assess the Effects of MEDI4736 following concurrent chemoradiation in
Patients with Stage III Unresectable Non-Small Cell Lung Cancer.
Patients with Stage III Unresectable Non-Small Cell Lung Cancer.
A Phase III, Randomised, Double-blind, Placebo-controlled, Multi-centre, International Study
of MEDI4736 as Sequential Therapy in Patients with Locally Advanced, Unresectable Non-Small
Cell Lung Cancer (Stage III) Who Have Not Progressed Following Definitive, Platinum-based,
Concurrent Chemoradiation Therapy (PACIFIC)
of MEDI4736 as Sequential Therapy in Patients with Locally Advanced, Unresectable Non-Small
Cell Lung Cancer (Stage III) Who Have Not Progressed Following Definitive, Platinum-based,
Concurrent Chemoradiation Therapy (PACIFIC)
Inclusion Criteria:
1. Age at least 18 years.
2. Documented evidence of NSCLC (locally advanced, unresectable, Stage III)
3. Patients must have received at least 2 cycles of platinum-based chemotherapy
concurrent with radiation therapy.
4. World Health Organisation (WHO) Performance Status of 0 to 1.
5. Estimated life expectancy of more than 12 weeks.
Exclusion Criteria:
1. Prior exposure to any anti-PD-1 or anti-PD-L1 antibody.
2. Active or prior autoimmune disease or history of immunodeficiency.
3. Evidence of severe or uncontrolled systemic diseases, including active bleeding
diatheses or active infections including hepatitis B, C and HIV.
4. Evidence of uncontrolled illness such as symptomatic congestive heart failure,
uncontrolled hypertension or unstable angina pectoris.
5. Any unresolved toxicity CTCAE >Grade 2 from the prior chemoradiation therapy.
6. Active or prior documented inflammatory bowel disease (eg, Crohn's disease, ulcerative
colitis).
We found this trial at
60
sites
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