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Status unknownNCT00514072Updated Aug 9, 2012

Vaccine Therapy in Treating Patients With Stage D0 Prostate Cancer

A Phase 2 interventional study of BCG vaccine and prostate cancer vaccine ONY-P1 in Prostate Cancer, sponsored by Kael-GemVax Co., Ltd.. Status unknown at 1 site in United States. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-08-09.

Sponsored by Kael-GemVax Co., Ltd. · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2012), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
54
Allocation
Randomized
Ages
18 Years and older
Sex
Male
01

Study summary

RATIONALE: Vaccines made from tumor cells may help the body build an effective immune response to kill tumor cells.

PURPOSE: This randomized phase II trial is studying vaccine therapy to see how well it works compared with a placebo in treating patients with stage D0 prostate cancer.

Read the detailed description

OBJECTIVES:

Primary

  • To determine whether ONY-P1 vaccine can increase the time to PSA-defined progression in patients with androgen-dependent stage D0 prostate cancer.

Secondary

  • To evaluate all toxicities related to ONY-P1 vaccine.
  • To compare the immunologic response in patients treated with ONY-P1 vaccine vs placebo.
  • To evaluate PSA kinetics (doubling time/velocity) of treatment.
  • To evaluate time to testosterone recovery following limited androgen ablation.

OUTLINE: Patients are stratified according to estimated PSA doubling time (\< 12 months vs ≥ 12 months).

Patients receive goserelin subcutaneously once. Approximately 3 months later, patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive ONY-P1 vaccine with BCG intradermally on days 1 and 15. Patients then receive ONY-P1 vaccine alone on day 29 and then every 4 weeks for up to 12 months in the absence of disease progression or unacceptable toxicity.
  • Arm II: Patients receive placebo vaccine intradermally on days 1, 15, and 29 and then every 4 weeks for up to 12 months in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed periodically for up to 15 years.

02

Conditions studied

  • Prostate Cancer

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Keywords

  • stage IV prostate cancer
  • recurrent prostate cancer
03

In context

Prostatic Neoplasms

6,367 studies on the registry are indexed under Prostatic Neoplasms; 1,397 are open to participants now.

This study's planned enrollment of 54 is close to the median of 58 across 4,821 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Kael-GemVax Co., Ltd. is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histopathological documentation of prostate cancer

    • If no pathologic specimen is available, patients may enroll on study with a pathologist's report showing a histologic diagnosis of prostate cancer and a clinical course consistent with the disease
  • Biochemical progression, as defined by the following:

    • A rise in PSA of ≥ 2 ng/mL above the nadir (for patients previously treated with definitive radiotherapy or cryotherapy)
    • Two consecutive rises in PSA > 0.3 ng/mL (for patients previously treated with radical prostatectomy)
  • PSA ≤ 20 ng/mL
  • Testosterone ≥ lower limit of normal
  • Negative CT scan and bone scan for metastatic prostate cancer
  • No clinically active brain metastases

PATIENT CHARACTERISTICS:

  • ECOG performance status of 0-1
  • Life expectancy ≥ 6 months
  • Granulocyte count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 10 g/dL
  • Bilirubin ≤ 1.5 mg/dL OR total bilirubin ≤ 3.0 mg/dL (in patients with Gilbert's syndrome)
  • AST and ALT ≤ 2.5 times upper limit of normal
  • No other active malignancies within the past 60 months (with the exception of nonmelanoma skin cancer or carcinoma in situ of the bladder)
  • No life-threatening illnesses
  • No immunocompromised status due to any of the following:

    • HIV positivity
    • Active autoimmune diseases, such as Addison's disease, Hashimoto's thyroiditis, systemic lupus erythematosus, Sjögren syndrome, scleroderma, myasthenia gravis, Goodpasture syndrome, or active Grave's disease

      • Patients with a history of autoimmunity that has not required systemic immunosuppressive therapy or does not threaten vital organ function, including CNS, heart, lungs, kidneys, skin, or gastrointestinal tract, will be allowed
    • Other immunodeficiency diseases or iatrogenic immunodeficiency from drugs
  • No other serious medical illness that would interfere with the patient's ability to carry out the treatment program
  • No documented contraindication (allergy or severe reaction to BCG)

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • Recovered from all prior therapy, including surgery and radiotherapy (no toxicity ≥ grade 2)
  • No prior chemotherapy
  • No concurrent topical steroids (including steroid eye drops) or systemic steroids

    • Nasal or inhaled steroid use is permitted
  • No concurrent medications used for urinary symptoms, including 5-alpha reductase inhibitors (finasteride and dutasteride)
  • No concurrent alternative medications known to alter PSA (e.g., phytoestrogens or saw palmetto)
  • No other concurrent hormonal therapy
  • No other concurrent anticancer treatment, including chemotherapy, systemic glucocorticoids, radiotherapy, major surgical procedures for prostate cancer, or nonprotocol-related immunotherapy
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Masking
Double (Participant, Investigator)
Enrollment
54 participants (estimated)

Study arms

  • Experimental
    Arm I

    Patients receive ONY-P1 vaccine with BCG intradermally on days 1 and 15. Patients then receive ONY-P1 vaccine alone on day 29 and then every 4 weeks for up to 12 months in the absence of disease progression or unacceptable toxicity.

    Biological: BCG vaccine · Biological: prostate cancer vaccine ONY-P1

  • Placebo comparator
    Arm II

    Patients receive placebo vaccine intradermally on days 1, 15, and 29 and then every 4 weeks for up to 12 months in the absence of disease progression or unacceptable toxicity.

    Other: placebo

Interventions

  • BiologicalBCG vaccine

    given intradermally

  • Biologicalprostate cancer vaccine ONY-P1

    given intradermally

  • Otherplacebo

    given intradermally

06

What researchers measure

Primary outcomes

  1. Time to PSA progression

Secondary outcomes

  1. Toxicity

  2. Immunologic response as assessed by ELISPOT assay

  3. PSA kinetics (doubling time/velocity) of treatment

  4. Time to testosterone recovery

07

Study locations

1 site
  • Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office
    Bethesda, Maryland 20892-1182, United States
08

References and documents

Publications

  • Aragon-Ching JB, Williams KM, Gulley JL. Impact of androgen-deprivation therapy on the immune system: implications for combination therapy of prostate cancer. Front Biosci. 2007 Sep 1;12:4957-71. doi: 10.2741/2441. PubMed 17569623 ↗
  • Huang J, Jochems C, Talaie T, Anderson A, Jales A, Tsang KY, Madan RA, Gulley JL, Schlom J. Elevated serum soluble CD40 ligand in cancer patients may play an immunosuppressive role. Blood. 2012 Oct 11;120(15):3030-8. doi: 10.1182/blood-2012-05-427799. Epub 2012 Aug 28. PubMed 22932804 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00514072
Lead sponsor
Kael-GemVax Co., Ltd.
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Aug 9, 2007
Start date
Mar 2007
Primary completion
Sep 2012 (estimated)
Last update
Aug 9, 2012

Study contacts

James L. Gulley, MD, PhD, FACP
principal investigator · National Cancer Institute (NCI)
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2012. You cannot join it, but the record below documents what was studied.

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