A Study of the IGF-1R Inhibitor AXL1717 in Combination With Gemcitabine HCL and Carboplatin to Treat Non-small-cell Lung Cancer (NSCLC)

NCT ID: NCT01466647

Last Updated: 2012-11-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-31
• Study Completion Date: 2012-09-30

Brief Summary

This is a open single-center, explorative, Phase I pilot dose finding study including patients treated with AXL1717 in addition to standard chemotherapy of gemcitabine HCL and carboplatin.

Detailed Description

Open single-center, explorative, Phase I pilot study including patients treated with AXL1717 in addition to standard chemotherapy of gemcitabine HCL and carboplatin. Patients will be treated within the study for 2 treatment cycles of 3 weeks each. Survival data will be obtained. Tumor assessment will be conducted at baseline and then at the end of the study period. Concomitant supportive therapies will be allowed.

Conditions

Non Small Cell Lung Cancer

Keywords

NSCLC

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

AXL1717 in combination with Gemcitabine HCL and Carboplatin

AXL1717 in combination with Gemcitabine HCL and Carboplatin

Group Type: OTHER

AXL1717

Intervention Type: DRUG

A repeated BID treatment for 14 days, followed by a 7 day observation period for two treatment periods

Interventions

AXL1717

A repeated BID treatment for 14 days, followed by a 7 day observation period for two treatment periods

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. At least 18 years of age.

2. Histologically or cytologically confirmed diagnosis of locally advanced, or metastatic squamous non-small-cell lung cancer (stage IIIB or IV) and scheduled for treatment with cytotoxic chemotherapy (Gemcitabine HCL/Carboplatin)

3. Preserved major organ functions, i.e:

• B-Leukocyte count ≥ 3.0 x 109/L
• B-Neutrophil count ≥ 1.5 x 109/L
• B-Platelet count ≥ 75 x109/L
• B-Haemoglobin ≥ 100 g/L (transfusions are allowed)
• P-Total bilirubin level ≤ 1.5 times the upper institutional limit of the "normal" (i.e. reference)range
• P-ASAT or P-ALAT ≤ 2.5 times upper institutional limit of the "normal" range, ≤5 times if liver metastases have been documented
• P-Creatinine ≤ 1.5 times upper institutional limit of the "normal" range
• 12-lead ECG with normal tracings; or clinically nonsignificant changes that did not require medical intervention

4. Signed written informed consent.

Exclusion Criteria

• The presence of any of the following criteria will exclude the patient from participating in the study:

• Ongoing infection or other major recent or ongoing disease that, according to the investigator, poses an unacceptable risk to the patient
• Grade 3 or higher constipation within the past 28 days or grade 2 constipation within the past 14 days before randomization. (Patients with grade 2 constipation within the past 14 days could be re-screened if constipation decreases to ≤ grade 1 with optimal management of constipation.)
• Known malignancy in Central Nervous System (CNS)
• Disease and dementia and neuropathy grade more than 1
• Other active malignancy during the previous 3 years
• Major surgical procedure within 4 weeks
• Prior anti-tumor therapy apart from radiation therapy
• Women Of Child Bearing Potential (WOCBP) - For purposes of this study, WOCBP include any female who has experienced menarche and who is not postmenopausal. Post menopause is defined as: Amenorrhea ≥ 12 consecutive months without another cause
• Pregnancy or lactation
• Current participation in any other interventional clinical trial
• Performance status > ECOG 2 after optimization of analgesics
• Life expectancy less than 3 months
• Contraindications to the investigational product, e.g. known or suspected hypersensitivity.
• Lack of suitability for participation in the trial, for any reason, as judged by the Investigator.

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

Sponsors

Axelar AB

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michael Bergqvist, M.D., Ph.D

Role: PRINCIPAL_INVESTIGATOR

Uppsala University Hospital, Sweden

Locations

KFUE

Uppsala, , Sweden

University Hospital

Uppsala, , Sweden

Countries

Sweden

Other Identifiers

AXL004

Identifier Type: -

Identifier Source: org_study_id