Phase Ib/II Study of MEDI4736 Evaluated in Different Combinations in Metastatic Pancreatic Ductal Carcinoma

Completed · Phase 1/Phase 2

Conditions studied: Metastatic Pancreatic Ductal Adenocarcinoma

In brief

A Phase Ib and II Open-Label, Multi-Center Study of MEDI4736 Evaluated in Different Combinations (with chemotherapy or AZD5069) in Patients with Metastatic Pancreatic Ductal Adenocarcinoma

Key facts

Study ID

NCT02583477

Run by

AstraZeneca

People needed

23

Starts

2016-03-25

Expected to finish

2018-07-09

Last updated by the study team

2019-08-14

Who can join

Age: 18 and older, up to 130. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically or cytologically confirmed metastatic PDAC, no more than 1 prior chemotherapy regimen or treatment-naïve patients
• Eastern Cooperative Oncology Group 0 or 1
• At least 1 lesion, not previously irradiated, that can be accurately measured at baseline as ≥10 mm in the longest diameter (except lymph nodes, which must have short axis ≥15 mm) with computed tomography (CT) or magnetic resonance imaging (MRI) scan and that is suitable for accurate repeated measurements
• MEDI4736 + nab-paclitaxel + gemcitabine chemotherapy cohort: treatment-naïve patients with metastatic PDAC who have received no previous systemic chemotherapy 5 MEDI4736 + Cohort: Patient should receive no more than 1 prior systemic chemotherapy regimen.
• Life expectancy ≥ 12 weeks. 7. ECOG PS of 0 or 1 8. Adequate organ and bone marrow function 9. Ability to undergo during screening a tumor biopsy that is adequate for biomarker analysis.

You may not qualify if…

• Any concurrent chemotherapy, investigational product , biologic, or hormonal therapy for cancer treatment.
• Receipt of any investigational anticancer therapy within 28 days or 5 half-lives, whichever is shorter, prior to the first dose of study treatment.
• Major surgical procedure within 21 days prior to the first dose of IP.
• Patients weighing less than 30 kg
• History of leptomeningeal carcinomatosis
• Ascites requiring intervention
• Any unresolved toxicity NCI CTCAE Grade ≥2 from previous anticancer therapy
• Current or prior use of immunosuppressive medication within 14 days of first dose
• Brain metastases or spinal cord compression.
• Medi4736+AZD5069 Cohort only: received any potent and moderate cytochrome CYP3A4 inhibitors, potent and moderate CYP3A4 inducers, P-gp substrates, BCRP substrates, sensitive CYP2B6 substrates, warfarin and coumarin derivatives, or herbal supplements within 14 days of the first dose of study treatment
• Uncontrolled intercurrent illness
• Other malignancy within 5 years except for noninvasive malignancies
• Mean QT interval ≥470 ms
• Active infection
• Receipt of live attenuated vaccine within 30 days prior to the first dose of IP
• Female patients who are pregnant or breastfeeding, or male or female patients of reproductive potential who are not employing an effective method of birth control
• Prior exposure to immune-mediated therapy
• Known allergy or hypersensitivity to IP formulations or to other human monoclonal antibodies

Where it is running

• Research Site — Rochester, New York, United States
• Research Site — Cambridge, United Kingdom
• Research Site — Glasgow, United Kingdom
• Research Site — London, United Kingdom
• Research Site — London, United Kingdom
• Research Site — Manchester, United Kingdom
• Research Site — Metropolitan Borough of Wirral, United Kingdom

Full record on ClinicalTrials.gov

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