A Phase 1/2 Study of HS-410 in Patients With Non-Muscle Invasive Bladder Cancer After TURBT
Status: | Completed |
---|---|
Conditions: | Cancer, Cancer, Bladder Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/23/2019 |
Start Date: | December 2013 |
End Date: | April 2018 |
A Phase 1/2, Placebo-Controlled, Randomized Study to Evaluate the Safety, Immune Response and Clinical Activity of HS-410 in Patients With Non-Muscle Invasive Bladder Cancer Who Have Undergone Transurethral Resection of Bladder Tumor (TURBT)
This study is a two part study: Phase I and Phase II. The Phase 1 portion is an open-label,
safety study. Patients will have previously received 3-6 instillations of weekly intravesical
Bacillus Calmette-Guerin (BCG) induction therapy (as standard of care) followed by low dose
intradermal (1*10^6 cells) HS-410 monotherapy. In Phase 2, patients will be assigned to
treatment groups based on whether they will receive induction BCG in the typical post-TURBT
window. If the investigator plans to administer BCG, patients will be randomized to one of
three blinded (physician-patient), placebo-controlled groups and receive either intradermal
placebo or low dose (1*10^6 cells) or high dose (1*10^7 cells) vesigenurtacel-L in
combination with induction and maintenance intravesical BCG. If patients will not receive
BCG, they will be enrolled into an open-label, non-randomized group and receive high dose
(1*10^7 cells) intradermal HS-410 monotherapy.
safety study. Patients will have previously received 3-6 instillations of weekly intravesical
Bacillus Calmette-Guerin (BCG) induction therapy (as standard of care) followed by low dose
intradermal (1*10^6 cells) HS-410 monotherapy. In Phase 2, patients will be assigned to
treatment groups based on whether they will receive induction BCG in the typical post-TURBT
window. If the investigator plans to administer BCG, patients will be randomized to one of
three blinded (physician-patient), placebo-controlled groups and receive either intradermal
placebo or low dose (1*10^6 cells) or high dose (1*10^7 cells) vesigenurtacel-L in
combination with induction and maintenance intravesical BCG. If patients will not receive
BCG, they will be enrolled into an open-label, non-randomized group and receive high dose
(1*10^7 cells) intradermal HS-410 monotherapy.
Inclusion Criteria:
- Histologically or cytologically confirmed non-muscle invasive bladder cancer [Ta, T1
or Tis (CIS)] that has been removed by transurethral resection
- Either: (i) high-risk disease, defined as T1 and/or high-grade and/or CIS or (ii)
intermediate-risk disease, defined as Ta low-grade with at least 3 of the following 4
risk factors: multiple tumors, tumor size > 3cm, early recurrence (<1 year from
previous staging procedure), or recurrence with a frequency of more than once in any
12 month period
- Not have received bacillus Calmette-Guérin (BCG) or have completed previous BCG
treatment > 12 months prior to the baseline staging procedure.
- Phase 2 Arms 1-3: Suitable to receive a 6-week course of BCG in the adjuvant setting
within 6 weeks following TURBT. Phase 2 Arm 4: Suitable for monotherapy vaccine
administration post-TURBT. For Phase 1 only: Has previously received 3-6 weekly doses
of BCG.
- Adequate laboratory parameters
Exclusion Criteria:
- Human immunodeficiency virus (HIV) infection or immunodeficiency disorders, either
primary or acquired
- Infections or intercurrent illness requiring active therapy
- Any condition requiring active steroid or other immunosuppressive therapy
- Active malignancies within the past 12 months except negligible risk of metastasis or
death treated with expected curative outcome.
- Prostate pelvic radiation within the past 12 months
- Significant cardiac impairment
- Current alcohol or chemical abuse, or mental or psychiatric condition precluding
protocol compliance
- Pregnant or nursing
- Allergy to soy, egg, or peanut products
- Receiving another investigational agent (30 day wash-out required prior to first dose)
- Neo-adjuvant therapy prior to baseline staging procedures for the current occurrence
of non-muscle invasive bladder cancer
- Prior treatment with a cancer vaccine for this indication
- Prior vaccination with BCG for tuberculosis disease
- Prior splenectomy
We found this trial at
19
sites
660 S Euclid Ave
Saint Louis, Missouri 63110
Saint Louis, Missouri 63110
(314) 362-5000
Washington University School of Medicine Washington University Physicians is the clinical practice of the School...
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Johns Hopkins University The Johns Hopkins University opened in 1876, with the inauguration of its...
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Montefiore Medical Center As the academic medical center and University Hospital for Albert Einstein College...
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University of North Carolina at Chapel Hill Carolina’s vibrant people and programs attest to the...
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University of Chicago One of the world's premier academic and research institutions, the University of...
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University of California at Los Angeles The University of California, Los Angeles (UCLA) is an...
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Univ of Minnesota With a flagship campus in the heart of the Twin Cities, and...
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823 82nd Parkway, Suite B
Myrtle Beach, South Carolina 29572
Myrtle Beach, South Carolina 29572
(843) 449-1010 ext.268
Carolina Urologic Research Center Carolina Urologic Research Center (CURC) has been recognized both nationally and...
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Thomas Jefferson University We are dedicated to the health sciences and committed to educating professionals,...
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