Phase 1 Study of GEN0101 in Patients With Recurrence of CRPC

NCT02502994 | Unknown Phase 1 DMC

• 1 other identifier: GEN0101-JM002
• Study Type: interventional
• Target: 12
• Locations: 1 country
• Sites: 1

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

Outcome Measures

Primary Outcomes (1)

• DLT (Dose Limiting Toxicity)

  To determine the appropriate dosing strategy for GEN0101 for castration resistant prostate cancer

  8 weeks

Secondary Outcomes (4)

• Number of participants with tumor shrinkage according to the RECIST.

  8 weeks

• Change from baseline in tumor marker (PSA: Prostate Specific Antigen, NSE: Neuron-specific enolase, CEA: Carcinoembryonic Antigen, and CA19-9: Carbohydrate Antigen19-9) at Cycle 1, Week 4 and at Cycle 2, Week 4.

  8 weeks

• Change from baseline in prostate histological evaluation at Cycle2, Week2.

  8 weeks

• Change from baseline in induction of antitumor immunity (NK cell activity, IL-6 and IFN-gamma) at Cycle1, Week 2 and Week 4 and at Cycle2, Week 2 and Week 4.

  8 weeks

Study Arms (1)

Intervention

OTHER

Single arm of the castration resistant prostate cancer

Drug: GEN0101

Interventions

GEN0101 DRUG

Intervention

Eligibility Criteria

• Age: 20 Years - 85 Years
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients providing a written informed consent by voluntary agreement.
• Age 20 =\< and =\<85 years old at the time of informed consent
• Have a diagnosis of malignant tumor as confirmed by histology or cytology.
• 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
• Serum PSA \<100 ng/mL at the screening visit
• Expected survival period is more than 8 weeks after planned start date of investigational product
• ECOG Performance Status 0 or 1
• Have an injectable intraprostatic lesion confirmed by histologic examination
• 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

You may not qualify if:

• Have multiple brain metastases
• Positive result of the prick test of GEN0101
• Have serious complications such as uncontrolled active infection
• 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.
• Received another investigational medical product within 4 weeks before the informed concent
• 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
• Have an active autoimmune disease
• 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).
• Had a history of the autologous or homogeneous organ or tissue transplantation (Receiving immunosuppressive medication)
• 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
• Positive result of the hepatitis B surface antigen, HCV antibody or HIV test at the screening visit
• Inappropriate to be enrolled in this study judged by the investigators

Sponsors & Collaborators

• Norio Nonomura: lead

Study Sites (1)

Urology, Osaka University Hospital

Suita, Osaka, 565-0871, Japan

RECRUITING

Study Officials

• Norio Nonomura, MD

  Urology, Osaka University Hospital

  STUDY CHAIR

Central Study Contacts

Norio Nonomura, MD

CONTACT

+81668793531; nono@uro.med.osaka-u.ac.jp

Katsuhisa Saito

CONTACT

+81662108289; saitokt@dmi.med.osaka-u.ac.jp

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: May 12, 2015
• First Posted: July 20, 2015
• Study Start: May 1, 2015
• Primary Completion: December 1, 2016
• Last Updated: July 20, 2015

Record last verified: 2015-07

Locations

JP (1)