A Phase I/Ib Trial for the Evaluation of SAR260301 in Monotherapy or in Combination With Vemurafenib in Patients With Various Advanced Cancer

Neoplasm Malignant Clinical Trial

Official title:

A Phase I/Ib Study for the Evaluation of SAR260301, Administered Orally in Monotherapy in Patients With Advanced Solid Tumors or Lymphomas, and in Combination With Vemurafenib in Patients With Unresectable / Metastatic BRAF-mutated Melanoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01673737
• Other study ID #: TCD12739
• Secondary ID: U1111-1129-2696
• Status: Completed
• Phase: Phase 1
• First received: August 23, 2012
• Last updated: April 9, 2015
• Start date: August 2012
• Est. completion date: February 2015

Study information

• Verified date: April 2015
• Source: Sanofi
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Primary Objective:

Part A - Monotherapy:

• To determine the maximum tolerated dose (MTD) of SAR260301 administered as monotherapy and either on a once or twice daily schedule, to patients with advanced solid tumors or lymphomas.

Part B - Combination:

• To determine the maximum tolerated dose (MTD) of SAR260301 administered in combination with the recommended standard dosage of vemurafenib to patients with unresectable / metastatic v-raf murine sarcoma viral oncogene homolog B1 (BRAF)-mutated melanoma.

Secondary Objectives:

• To characterize the overall safety and tolerability profile of SAR260301 administered as monotherapy (Part A) and in combination with vemurafenib (Part B).

• To characterize the pharmacokinetic (PK) profile of SAR260301 administered as monotherapy (Part A) and in combination with vemurafenib (Part B) as well as vemurafenib PK in combination with SAR260301 (Part B)

• To evaluate food effect on SAR260301 PK (Part A)

• To assess preliminary antitumor activity according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1 criteria).

• To assess preliminary antitumor activity using volumetric computed tomography (CT) or magnetic resonance imaging(MRI)

• To evaluate the pharmacodynamic (PD) effects of SAR260301 on blood and tumor.

• To evaluate PK/PD relationships.

• To identify the recommended phase 2 dose of SAR260301 in combination with vemurafenib (RP2D) (Part B only)

• To assess potential induction effect of SAR260301 on cytochrome P450 (CYP) isoenzyme 3A (CYP3A) (Part A)

Description:

Study duration for one patient will include a period for inclusion (screening period) of up to 4 weeks, a treatment period of at least 4 weeks, and a end-of-study visit at 30 days following the last administration of study drug. The patient may continue treatment until disease progression, unacceptable toxicity or willingness to stop, followed by a minimum of 30-days follow-up.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 75
• Est. completion date: February 2015
• Est. primary completion date: February 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion criteria :

• Age =18 years old

• Locally advanced or metastatic solid tumor disease as well as lymphoma for which no alternative therapy is available (Part A)

• Unresectable / metastatic BRAF-mutated melanomas, progressing on BRAF inhibitor after no more than 4 months treatment or with only partial response (<50% change in tumor volume) after 4 months of treatment (Part B) or vemurafenib naive (Part B escalation phase only): anterior scans must be available for patients having received BRAF inhibitor prior to entry into the study.

• At least one measurable lesion by RECIST v1.1

• Archived primary tumor biopsies or surgical specimens, or biopsies of recurrence or metastasis, will be requested for all subjects for predictive markers of response analysis.

Exclusion criteria:

• ECOG performance status >1

• Concurrent treatment with any other anticancer therapy

• Patient with reproductive potential (female and male) who do not agree to use an accepted effective method of contraception during the study treatment period and for at least 6 months following completion of study treatment.

• Pregnancy or breast-feeding

• Any malignancy related to immunodeficiency virus (HIV) or solid organ transplant; history of known HIV, unresolved viral hepatitis.

• Subjects with brain metastases of non-central nervous system (CNS) primary tumors are excluded if their lesions are larger than 1 cm in the longest dimension, symptomatic or changed in size in the latest scan compared to the previous scan. Subjects must not require corticosteroid treatment or have received treatment for brain metastases for at least one month prior to study entry.

• Inadequate haematological function.

• Inadequate renal function.

• Inadequate liver function.

• Non-resolution of any prior treatment related toxicity to < Grade 2, except for alopecia according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.03.

• Any major surgery within the last 28 days.

• History of congenital platelet function defect or bleeding diathesis.

• Abnormal platelet function using platelet function assay PFA 100® including aggregation time >122 seconds using the collagen/ADP cartridge, and/or >183 seconds using the collagen/epinephrine cartridge.

• Current use of aspirin, clopidogrel, ticlopidine, prasugrel or ticagrelor.

• Abnormal coagulation parameters: Prothrombin time (PT)/ international normalized ratio (INR) or activated partial thromboplastin time (aPTT) >1.3X ULN. Prophylactic but not therapeutic anticoagulants are permitted.

• Any of the following within 6 months prior to study enrolment: peptic ulcer disease, erosive oesophagitis, or gastritis, infectious or inflammatory bowel disease, diverticulitis, GI perforation, intestinal obstruction and GI hemorrhage.

• Patients with history of chronic renal diseases, interstitial nephritis, or with uncontrolled or unresolved acute renal failure.

• Hemoptysis within the past 3 months.

• Patients with known Gilbert's syndrome.

• Prior hypersensitivity reaction or severe dermatologic reactions such as Steven's Johnsons syndrome and toxic epidermal necrolysis (TENS) to vemurafenib in Part B.

• Uveal melanoma as new primary malignancy in Part B

• Prior history or ongoing uveitis

• Mean QTc interval >470 msec (using QTcF formula) or any clinically significant QTc prolongation, history of Torsade de Pointes or malignant arrhythmias or conduction disturbances.

• Other clinically significant ECG abnormalities including 2nd degree (Mobitz Type II), familial history of long QT syndrome and 3rd degree atrioventricular block.

• Congestive heart failure

• Uncontrolled or untreated hypertension

• Uncorrectable serum abnormalities for the following electrolytes: potassium, magnesium and calcium.

• Medical conditions having to require concomitant administration of strong CYP3A4 inhibitors or inducers 2 weeks prior to study treatment or 5 elimination half-life of the drug, whichever is longest.

• Medical conditions requiring concomitant administration of medications with a narrow therapeutic window and metabolized by CYP1A2 or CYP2D6, and for which a dose reduction cannot be considered.

• Medical conditions requiring concomitant administration of medications susceptible to prolong QTc interval.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Neoplasm Malignant
• Neoplasms

Intervention

Drug:
• SAR260301
Pharmaceutical form: film-coated tablets Route of administration: oral
• Vemurafenib
Pharmaceutical form: film-coated tablets Route of administration: oral

Locations

Country	Name	City	State
Canada	Investigational Site Number 124001	Toronto
United States	Investigational Site Number 840001	Boston	Massachusetts
United States	Investigational Site Number 840101	Boston	Massachusetts
United States	Investigational Site Number 840002	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Sanofi

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximal tolerated dose (MTD) of SAR260301 in monotherapy (Study Part A)		Day 28	Yes
Primary	Maximal tolerated dose (MTD) of SAR260301 in combination with vemurafenib (Study Part B)		Day 28	Yes
Secondary	Number of patients with treatment emergent events		Up to 2 years	Yes
Secondary	Assessment of PK parameters for SAR260301 and vemurafenib, including tmax, Cmax, AUC, Rac (Day 28/Day1), half-life, CL, Ctrough		4 weeks	Yes
Secondary	Assessment of PK parameters for SAR260301 including tmax, Cmax, AUC fasting and fed (food effect)(Only part A)		Up to 8 weeks	Yes
Secondary	Assessment of urine excretion of SAR2690301 (Part A)		12-24 hours at Day 28	No
Secondary	Assessment of potential for CYP induction (4beta-hydroxycholesterol)(Part A)		Up to 15 days	No
Secondary	Assessment of PK parameter Rac (Day 28/Day 1) on AUC and Cmax		4 weeks	No
Secondary	Assessment of PD parameter Serine/threonine protein kinase Akt (AKT) phosphorylation in blood platelets		4 weeks	No
Secondary	Assessment of PD parameter AKT phosphorylation in tumor (expansion phase only)		15 days	No
Secondary	Assessment of preliminary antitumor activity as documented by tumor response (defined by RECIST1.1 criteria for solid tumors, international working group (IWG) and revised response for lymphomas, and tumor markers when relevant)		Up to 2 years	No