A phase 3 study to compare as first line therapy efficacy and safety of masitinib in combination with gemcitabine, followed as second line treatment by AB1010 in combination with Folfiri 3 in the treatment of patients with non resectable locally advanced or metastatic pancreatic cancer

Phase 3

Conditions: Health Condition 1: null- Non resectable locally advanced or metastatic pancreatic cancer

Registration Number: CTRI/2015/10/006265

Lead Sponsor: AB Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: Not specified

Target Recruitment: 550

Inclusion Criteria

1.Histologically or cytologically confirmed adenocarcinoma of the pancreas

2.Patient with pain related to the disease, as assessed by the investigator and the patient:-Pain related to the disease as assessed by the investigator is defined as clinical and documented evaluation by the investigator during physical examinations at screening and/or baseline.

-Pain, as assessed by the patient is defined as at least one value out of two values > 5mm on Visual Analogic Scale at screening or baseline. Visual Analogic scale consists in the visual representation of pain amplitude as perceived by the patient. The amplitude is represented by a 100mm long line having no reference marks. One extremity indicates an absence of pain (0 value) and the other the worst imaginable pain (100 value). OR Patient treated with opioid analgesics at a dose >= 1 mg/kg/day (morphinic equivalent). OR Patients with â??genetic fingerprint of aggressivenessâ??:

3.Chemotherapy naÃ¯ve patient for the advanced/metastatic disease

4.Documented decision justifying non eligibility for surgical resection.

5.Patient with measurable tumor lesions with longest diameter >= 20 mm using conventional techniques or >= 10 mm with spiral CT scan according to RECIST 1.1

6.Patient with ECOG <= 1

7.Patient with adequate organ functions:

-Absolute neutrophils count (ANC) >= 1.5 x 109/L

-Haemoglobin >= 10 g/dL

-Platelets (PTL) >= 75 x 109/L

-AST/ALT <= 5 x ULN

-Gamma GT <= 5 x ULN

-Bilirubin <= 3 x ULN

-Normal Creatinine or if abnormal creatinine, creatinine clearance >= 50 mL/min (Cockcroft and Gault formula)

-Albumin > 1x LLN

-Proteinuria < 30 mg/dL (1+) on the dipstick. If proteinuria is >= 1+ on the dipstick, 24 hours proteinuria must be < 1.5g/24 hours

-Patient with life expectancy > 3 months

8.Male or female patient, age - 18 years

9.Patient with a BMI > 18 kg/mÂ² and >40 kg

10.Male patient or female patient of childbearing potential must agree to use two methods (one for the patient and one for the partner) of medically acceptable forms of contraception (with failure rate < 1%) during the study and for 3 months after the last treatment intake.

11.Female patient of childbearing potential must have a negative pregnancy test at screening and baseline.

12.Patient able and willing to comply with study procedures as per protocol

13.Patient able to understand the patient card and to follow the patient card procedures, in case of signs or symptoms of severe neutropenia or severe cutaneous toxicity during the first 2 months of treatment.

14.Patient able to understand, sign, and date the written informed consent form at the screening visit prior to any protocol-specific procedures are performed. If the patient is deemed by the treating physician to be cognitively impaired or questionably impaired in such a way that the ability of the patient to give informed consent is questionable, the designated legal guardian must sign the informed consent.

Exclusion Criteria

1.Patient treated for a cancer other than pancreatic cancer within 5 years before enrolment, with the exception of basal cell carcinoma or cervical cancer in situ 2.Patient with no pain related to the disease (as defined in the inclusion criterion number 2)and no genetic fingerprint of aggressiveness 3.Patient with ECOG >= 2 4.Patient with active central nervous system metastasis or with history of CNS metastasis 5.Patient presenting with cardiac disorders defined by at least one of the following conditions: - Patient with recent cardiac history (within 6 months) of:

- Acute coronary syndrome - Acute heart failure (class III or IV of the NYHA classification)- Significant ventricular arrhythmia(persistent ventricular tachycardia, ventricular fibrillation, resuscitated sudden death) . Patient with cardiac failure class III or IV of the NYHA classification . Patient with severe conduction disorders which are not prevented by permanent pacing (atrio-ventricular block 2 and 3, sino-atrial block) . Syncope without known aetiology within 3 months

. Uncontrolled severe hypertension according to the judgement of the investigator, or symptomatic hypertension

6. Patient with history of poor compliance or history of drug/alcohol abuse, or excessive alcohol beverage consumption that would interfere with the ability to comply with the study protocol, or current or past psychiatric disease that might interfere with the ability to comply with the study protocol or give informed consent

7. Pregnant, intent to be pregnant, or nursing female patient

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Overall survival (OS)Timepoint: Overall survival (OS)

Secondary Outcome Measures

Name	Time	Method
PFS rate every 8 weeks and TTS rate every 8 weeks and Best response along study: Complete response (CR) rate, Partial Response (PR) rate, Progressive disease (PD) every 8 weeksTimepoint: Survival rate every 24 weeks