A Dose Escalation Study of MM-398 Plus Irinotecan in Patients With Unresectable Advanced Cancer

This is a dose-finding and therapeutic exploratory phase Ib multi-center, open label study of MM-398 plus irinotecan in two different settings:

• Group A : patients with unresectable advanced non-colorectal cancer who should receive only MM-398 and irinotecan
• Group B : patients with unresectable metastatic colorectal cancer who should receive MM-398 and irinotecan combined with leucovorin, 5-fluorouracil and bevacizumab.

These groups will be enrolling in parallel. Pharmacokinetic and biomarker sampling will also be performed.

There are three periods to this study :

Screening period (up to -28d): patients undergo screening assessments to determine the eligibility for the study

MM-398 treatment period (C1D1 until safety evaluation/progression): patients receive treatment every 2 weeks and undergo biopsies and other required assessments. The treatment period is divided into a maximum of 3 dose levels

Follow up period: patients will be followed-up 30 days after their last dose of MM-398 for final safety assessments, and every 2 months thereafter for overall survival follow-up

Inclusion criteria

• Age 18 - 75 years
• Histologically proven carcinoma,
• Documented advanced or metastatic disease not suitable for complete surgical resection
• Measurable or evaluable lesions according to RECIST v1.1 criteria
• ECOG performance status 0 - 1
• Adequate Bone marrow reserves as evidenced by:

• Absolute Neutrophil Count (ANC) ≥1.5 x 109/L without the use of hematopoietic growth factors
• platelets ≥ 100 x 109/L
• hemoglobin > 9 g/dL (may be transfused to maintain or exceed this level)
• International Normalized Ratio (INR) ≤1.5; aPTT<1.5 x upper normal limit (UNL); EXEMPTION: patients on full anticoagulation therapy due to Venous Thromboembolism (VTE) must have an in-range INR (usually between 2 and 3).
• Adequate renal function as evidenced by:

• serum creatinine: < 150µmol/l
• calculated creatinine clearance > 50ml/min. (recommendation: to be calculated according to the MDRD formula)
• Total bilirubin < 1.0 x upper normal limit (UNL)
• Normal ECG or ECG without any clinically significant findings
• Regular follow-up feasible. A registered patient must be treated and followed at the participating center.
• Able to understand and sign an informed consent
• No contraindication to any study drugs
• Registration in a national health care system (CMU included for France). NB.: prior exposure to irinotecan is allowed, except for irinotecan-refractory patients (i.e. exclusion criteria)

Exclusion criteria

• Active central nervous system metastases (indicated by clinical symptoms, cerebral edema, steroid requirement, or progressive disease)
• Bone-only disease
• Clinically significant gastrointestinal (GI) disorder including hepatic disorders, bleeding, inflammation, GI obstruction, or diarrhea > grade 1
• Patients refractory to irinotecan (i.e. prior exposure to irinotecan-based therapy with progressive disease as best response)
• Known Dose Limiting Toxicity (DLT) responses to irinotecan
• Patients known to be homozygous for UGT1A1 *28
• History of any second malignancy in the last 3 years; patients with prior history of in-situ cancer or basal or squamous cell skin cancer are eligible. Patients with a history of other malignancies are eligible if they have been continuously disease-free for at least 3 years
• Prior exposure to MM-398
• Known hypersensitivity to any of the components of MM-398, or other liposomal products
• Concurrent illnesses that would be a relative contraindication to trial participation such as active cardiac or liver disease

• Severe arterial thromboembolic events (myocardial infarction, unstable angina pectoris, stroke) less than 6 months before inclusion
• NYHA Class III or IV congestive heart failure, ventricular arrhythmias
• Chronic inflammatory bowel disease and/or bowel obstruction
• Active infection or an unexplained fever >38.5°C during screening visits or on the first scheduled day of dosing (at the discretion of the investigator, patients with tumor fever may be enrolled), which in the investigator's opinion might compromise the patient's participation in the trial or affect the study outcome
• Prior chemotherapy administered within 3 weeks, or within a time interval less than at least 5 half-lives of the agent, whichever is longer, prior to the first scheduled day of dosing in this study
• Uncontrolled hypertension (defined as persistent systolic blood pressure >150 mmHg and/or diastolic blood pressure >100 mmHg), or history of hypertensive crisis, or hypertensive encephalopathy
• Received radiation therapy in the last 14 days
• Major surgery or traumatic injury within the last 28 days
• Any other medical or social condition deemed by the Investigator to be likely to interfere with a patient's ability to sign informed consent, cooperate and participate in the study, or interfere with the interpretation of the results including tutelage and guardianship
• Pregnant or breast feeding; females of child-bearing potential must test negative for pregnancy at the time of enrollment based on a urine or serum pregnancy test. Both male and female patients of reproductive potential must agree to use a reliable method of birth control, during the study and for 6 months following the last dose of study drug.
• Concomitant administrations use with St John Worth, or CYP3A4 inducing anticonvulsants (phenytoin, Phenobarbital, carbamazepine), ketoconazole, itraconazole, troleandomycin, erythromycin, diltiazem and verapamil
• Concomitant administration of live attenuated virus vaccine such as yellow fever vaccine
• Known dihydropyrimidine dehydrogenase (DPD) deficiency
• Known active hepatitis B or C and/or active or chronic human immunodeficiency virus (HIV)