A Randomized Phase 2 Study of ARQ 197 Versus Gemcitabine in Treatment-Naïve Patients With Unresectable Locally Advanced or Metastatic Pancreatic Adenocarcinoma

NCT ID: NCT00558207

Last Updated: 2013-02-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-11-30
• Study Completion Date: 2008-04-30

Brief Summary

This is a multi-center, open-label randomized phase 2 study designed to assess the progression free survival (PFS) of patients with untreatment and unresectable pancreatic cancer following treatment with either ARQ 197 or gemcitabine. The study will also evaluate other efficacy and safety endpoints including overall response rate, overall survival and adverse events in the two treatment arms.

Detailed Description

This is a multi-center, open-label randomized phase 2 study designed to evaluate the PFS of treatment-naïve patients with unresectable (locally advanced or metastatic) pancreatic adenocarcinoma following treatment with either ARQ 197 (ARQ arm) or gemcitabine alone (GEM arm). The study will also evaluate other efficacy and safety parameters including ORR, OS and adverse events in the two treatment arms. Patients randomly assigned to the GEM arm will receive gemcitabine alone. Patients assigned to the ARQ arm will receive oral ARQ 197 alone.

ARQ 197 is an investigational oral drug supplied as capsules in multiple strengths. For the study initial shipment the capsules were 120 mg each, 30 count. In the ARQ arm, patients will take 120 mg of ARQ 197 twice daily, once in the morning and once in the evening one hour prior to or two hours after a meal. ARQ 197 treatment will be continued until unacceptable toxicity, documented progression of disease, or another discontinuation criterion is met.

Gemcitabine is a commercially available drug for the treatment of patients with locally advanced or metastatic adenocarcinoma of the pancreas. In the GEM arm, gemcitabine will be administered by intravenous infusion over 30 minutes at a dose of 1000 mg/m2. The dosing schedule of gemcitabine will be once weekly for the first cycle (4 weeks), then once weekly for 3 consecutive weeks followed by a week of rest for each subsequent cycle. Gemcitabine therapy will be continued until unacceptable toxicity, documented progression of disease, or another discontinuation criterion is met.

A treatment cycle is defined as 28 days for both treatment arms. Cycles may be repeated every 4 weeks (28 days) based on toxicity and response. The assigned treatment should continue until unacceptable toxicity, disease progression (clinical or radiological) or another discontinuation criterion is met.

Tumor evaluations: Tumor evaluations will be performed in 8-week intervals. Tumor response (complete response, partial response, stable disease, progressive disease and ORR) will be evaluated using Response Evaluation Criteria in Solid Tumors (RECIST).

Progression-free survival: The time of disease progression-free will be calculated from randomization until disease progression per RECIST or death due to any cause. Patients who are alive and progression free will be censored at the date of their last tumor evaluation.

Overall survival: Overall survival time will be calculated from the date of randomization until death due to any cause.

Safety assessments: Data on vital signs, physical examination, adverse events, serum chemistry, hematological laboratory tests, and electrocardiograms will be collected.

This study is designed to establish potential efficacy of ARQ 197 in treatment naive pancreatic cancer patients in a controlled, randomized study. The sample size of 30 Evaluable patients per treatment group is considered adequate to provide meaningful estimates of the PFS and ORR and OS rates, however, this study is not powered to show statistically significant differences between the treatment groups. Therefore, the analyses will be primarily descriptive in nature. Taking into account an anticipated drop-out/loss-to-follow-up rate of 20%, the total sample size will be 72 patients.

Primary and secondary objectives will be analyzed in the two treatment arms using appropriate patient populations and statistical methods.

Conditions

Pancreatic Neoplasms

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

ARQ 197

Group Type: EXPERIMENTAL

ARQ 197

Intervention Type: DRUG

120 mg capsule administered twice daily for 240 mg total daily dose

2

Gemcitabine

Group Type: ACTIVE_COMPARATOR

gemcitabine

Intervention Type: DRUG

1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 4 weeks for the first 28 days (cycle). Each subsequent cycle will consist of 1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 3 weeks with no drug administered in the 4th week.

Interventions

ARQ 197

120 mg capsule administered twice daily for 240 mg total daily dose

Intervention Type: DRUG

gemcitabine

1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 4 weeks for the first 28 days (cycle). Each subsequent cycle will consist of 1000 mg/m2 administered as an intravenous infusion over 30 minutes once weekly for 3 weeks with no drug administered in the 4th week.

Intervention Type: DRUG

Other Intervention Names

Gemzar

Eligibility Criteria

Inclusion Criteria

1. Able to provide signed and dated informed consent prior to study-specific screening procedures

2. ≥ 18 years old

3. Histologically or cytologically confirmed locally advanced or metastatic unresectable pancreatic adenocarcinoma

4. Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)

5. Karnofsky performance status (KPS) ≥ 70%

6. Male or female patients of child-producing potential must agree to use double barrier contraception, oral contraceptives or avoidance of pregnancy measures during the study and for 90 days after the last day of treatment

7. Females of childbearing potential must have a negative serum pregnancy test

8. Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 × upper limit of normal (ULN) or ≤ 5 × ULN with metastatic liver disease

9. Hemoglobin ≥ 10 g/dl

10. Total bilirubin ≤ 1.5 × ULN

11. Serum creatinine ≤ 1.5 x ULN

12. Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L

13. Platelets ≥ 100 x 10^9/L

Exclusion Criteria

1. Received any prior therapy for the treatment of their pancreatic malignancy (including chemotherapy, immunotherapy, vaccines, monoclonal antibodies, major surgery, or irradiation, whether conventional or investigational)

2. Central nervous system metastases

3. Pregnant or breastfeeding

4. Significant gastrointestinal disorder, in the opinion of the Principal Investigator (e.g. Crohn's disease, ulcerative colitis, extensive gastric resection)

5. Unable or unwilling to swallow ARQ 197 capsules twice daily

6. Other cancer within the last five years, with the exception of adequately treated cone-biopsied in situ carcinoma of the cervix uteri or basal or squamous cell carcinoma of the skin

7. Significant co-morbid conditions that in the opinion of the Investigator would impair study participation

8. Known human immunodeficiency virus (HIV) or hepatitis C virus (HCV) infection

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Cezary Szczylik, PhD

Role: PRINCIPAL_INVESTIGATOR

Klinika Onkologii WIM

Janusz Pawlega, PhD

Role: PRINCIPAL_INVESTIGATOR

Oddzial Kliniczny Kliniki Onkologii

Piotr Koralewski, MD

Role: PRINCIPAL_INVESTIGATOR

Oddzial Chemioterapii Krakow

Emilia Filipczyk-Cisarz, MD

Role: PRINCIPAL_INVESTIGATOR

Oddzial Chemioterapii Dolnoslaskie Centrum Onkologii

Ewa Kilar, MD

Role: PRINCIPAL_INVESTIGATOR

Regionalny Szpital Specjalistyczny Latawiec

Piotr Sawrycki, MD

Role: PRINCIPAL_INVESTIGATOR

Oddzial Onkologii Klinicznej im L Rydygiera

Locations

Oddzial Kliniczny Kliniki Onkologii Szpital Uniwersytecki w Krakowie

Krakow, , Poland

Oddzial Chemioterapii, Wojewodzki Szpital Specjalistyczny

Krakow, , Poland

Oddział Onkologii Klinicznej, Regionalny Szpital Specjalistyczny "Latawiec"

Swidnica, , Poland

Oddział Onkologii Klinicznej SP ZOZ Wojewódzki Szpital Zespolony im. L. Rydygiera

Torun, , Poland

Klinika Onkologii WIM Warszawa

Warsaw, , Poland

Oddział Chemioterapii Dolnośląskie Centrum Onkologii

Wroclaw, , Poland

Countries

Poland

Other Identifiers

ARQ 197-205

Identifier Type: -

Identifier Source: org_study_id