Phase 1 Study of GEN0101 in Patients With Recurrence of CRPC

NCT ID: NCT02502994

Last Updated: 2015-07-20

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-05-31

Brief Summary

This study is designed to evaluate the safety and efficacy of a single injection of GEN0101 in patients with recurrence of castration resistant prostate cancer.

The subjects receive GEN0101 injection 4 times per two weeks (1st intratumoral injection and followed subcutaneous injection) and two weeks of observation as one cycle treatment period. Each subject receive two cycle treatment period.

Low dose group: 30,000m NAU per injection of GEN0101 High dose group: 60,000m NAU per injection of GEN0101 Each group included minimal 3 subjects.

Conditions

Castration Resistant Prostate Cancer

Study Design

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

Study Groups

Intervention

Single arm of the castration resistant prostate cancer

Group Type: OTHER

GEN0101

Intervention Type: DRUG

Interventions

GEN0101

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients providing a written informed consent by voluntary agreement.

2. Age 20 =< and =<85 years old at the time of informed consent

3. Have a diagnosis of malignant tumor as confirmed by histology or cytology.

4. Have a diagnosis of recurrence of castration resistant prostate cancer and meet the following condition

• Inapplicable to the standard treatment, ineffective through the criteria of the Prostate Cancer Clinical Trials Working Group (PCWG2) or refuse the standard treatment
• More than 6 week between the end date of the standard treatment and the registration date when the standard treatment has been ineffective

5. Serum PSA <100 ng/mL at the screening visit

6. Expected survival period is more than 8 weeks after planned start date of investigational product

7. ECOG Performance Status 0 or 1

8. Have an injectable intraprostatic lesion confirmed by histologic examination

9. The marrow function, liver function and the kidney function must be kept as follows at the screening visit (1) leukocyte >= 3,000/mcL (2) neutrophil >=1,500/mcL (3) platelet >=75,000/mcL (4) hemoglobin >=8.0 g/dL. (5) AST =<100 IU/L (6) ALT =<100 IU/L (7) total bilirubin =<2.5 mg/dL (8) serum creatinine =<2.5 mg/dL

Exclusion Criteria

1. Have multiple brain metastases

2. Positive result of the prick test of GEN0101

3. Have serious complications such as uncontrolled active infection

4. Received systemic chemotherapy, radiotherapy or immunotherapy within 6 weeks before the planned registration date However the hormone therapy except for the estramustine, enzalutamide and abiraterone, bisphosphonate and anti-RANKL antigen antibody is are not included in the systemic chemotherapy.

5. Received another investigational medical product within 4 weeks before the informed concent

6. Had a history of malignancy other than prostate cancer, except for the relapse-free and metastasis-free for more than 5 years after the last treatment at the registration

7. Have an active autoimmune disease

8. Receiving systemic administration of glucocorticosteroid which restrains immunity response, except for the administration for a long period (over 6 months) of the low dose (equivalent to under 10 mg/day oral prednisolone).

9. Had a history of the autologous or homogeneous organ or tissue transplantation (Receiving immunosuppressive medication)

10. PT(%) less than 10% of the lower limit of normal or APTT more than 1.5 times of the upper limit of normal of local reference range at the screening visit

11. Positive result of the hepatitis B surface antigen, HCV antibody or HIV test at the screening visit

12. Inappropriate to be enrolled in this study judged by the investigators

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Norio Nonomura

OTHER

Sponsor Role: lead

Responsible Party

Norio Nonomura

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Norio Nonomura, MD

Role: STUDY_CHAIR

Urology, Osaka University Hospital

Locations

Urology, Osaka University Hospital

Suita, Osaka, Japan

Site Status: RECRUITING

Countries

Japan

Central Contacts

Norio Nonomura, MD

Role: CONTACT

nono@uro.med.osaka-u.ac.jp

+81668793531

Katsuhisa Saito

Role: CONTACT

saitokt@dmi.med.osaka-u.ac.jp

+81662108289

Other Identifiers

GEN0101-JM002

Identifier Type: -

Identifier Source: org_study_id