Open Label, Dose Escalation Trial of Oral Eg5 Kinesin-spindle Inhibitor 4SC-205 in Patients With Advanced Malignancies

NCT ID: NCT01065025

Last Updated: 2015-04-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-01-31
• Study Completion Date: 2015-04-30

Brief Summary

The purpose of the study is to investigate safety and tolerability of repeated ascending oral doses of 4SC-205 in patients with advanced and incurable solid tumors or malignant lymphomas.

Conditions

Advanced and Incurable Solid Tumors; Malignant Lymphomas

Study Design

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

Study Groups

4SC-205

Group Type: EXPERIMENTAL

4SC-205

Intervention Type: DRUG

Repeated ascending oral doses of 4SC-205.

Interventions

4SC-205

Repeated ascending oral doses of 4SC-205.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• One or more evaluable target lesion according to RECIST (by CT-scan, MRI or calipers), of which at least one evaluable target lesion (proven by CT or MRI) has to be located in the lung.
• Progressive disease as defined by new or progressive lesions on CT-scan, MRI, bone scan or by increase of PSA.
• Histologically or cytologically documented diagnosis of primary or metastatic solid tumors or malignant lymphomas refractory to prior standard therapy or for which no standard therapy exists. Entry will include, but is not limited to patients with prostate and breast cancer refractory to hormone treatment, ovarian cancer, head and neck cancer, non-small cell lung cancer, bladder cancer, colorectal cancer, kidney cancer, malignant melanoma or malignant lymphoma. Patients who have refused standard therapies are also eligible.
• ECOG Performance Status 0-2.
• Acceptable liver, renal and bone marrow function.

Exclusion Criteria

• Prior treatment with other EG5 inhibitors.
• Antineoplastic therapy including chemotherapy, radiotherapy, endocrine therapy, immunotherapy or use of other investigational agents within the last 2 weeks or a longer period depending on the defined characteristics of the agents used (e.g. 6 weeks for mitomycin C or nitrosourea). Patients must have recovered from any treatment-related toxicity (except for alopecia, fatigue and grade 1 neurotoxicity) prior to registration.
• Patients with a history of other malignancies unless having undergone definitive treatment more than 5 years prior to entry into the study and without evidence of recurrent malignant disease, excluding patients with basal cell carcinoma of the skin; superficial carcinoma of the bladder; carcinoma of the prostate with a current PSA < 0.1 ng/ml; or cervical intraepithelial neoplasia.
• Patients with a history of significant cardiovascular, neurological, endocrine, gastrointestinal, respiratory or inflammatory illness.
• Patients with a history of, who were treated for, or who are suspected of having, hepatitis B, hepatitis C or HIV.

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

Sponsors

4SC AG

INDUSTRY

Sponsor Role: lead

Principal Investigators

Klaus Mross, PD Dr. med.

Role: PRINCIPAL_INVESTIGATOR

Klinik für Tumorbiologie an der Albert-Ludwigs-Universität Freiburg (KTB)

Locations

Universitätsklinikum Essen

Essen, , Germany

Klinik für Tumorbiologie an der Albert-Ludwigs-Universität Freiburg (KTB)

Freiburg im Breisgau, , Germany

Countries

Germany

Other Identifiers

4SC-205-1-2009

Identifier Type: -

Identifier Source: org_study_id