PAW: Study of Leukocyte Interleukin, Injection for Treatment of Perianal Warts
Study Details
Study Description
Brief Summary
Study is a dose escalation study. Fifteen patients will be enrolled in 2 treatment cohorts. Five participants (cohort A) will be treated with 200IU Multikine daily, 5 days/week for 2 weeks, off 2 weeks, then again 5 days/week for 2 weeks. If no serious adverse events are noted in cohort A patients, ten participants will be treated in cohort B. Cohort B participants will be treated the same as cohort A participants except that dose will be increased to 400IU Multikine per day.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
Study is a dose escalation study to determine the safety of Leukocyte Interleukin, Injection in treating men and women with perianal warts who are HIV/HPV co-infected. Fifteen patients will be enrolled in 2 treatment cohorts. Five participants (cohort A) will be treated with 200IU Multikine daily, 5 days/week for 2 weeks, off 2 weeks, then treated again 5 days/week for 2 weeks. If no serious adverse events are noted in cohort A patients, ten (10) participants will be treated in cohort B. Cohort B participants will be treated in the same manner as cohort A participants except that the dose will be increased to 400IU Multikine per day.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Arm A Cohort A - 200IU Leukocyte Interleukin, Injection 5 days/week x 2 weeks, off two weeks, then repeat 200IU 5 days/week x 2 weeks. |
Biological: Leukocyte Interleukin, Injection
Immunotherapy
Other Names:
|
| Experimental: Arm B Arm B - 400IU Leukocyte Interleukin, Injection 5 days/week x 2 weeks, off 2 weeks, 400IU 5 days/week x 2 weeks. |
Biological: Leukocyte Interleukin, Injection
Immunotherapy
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Wart characterization change [Time Frame: Days 0, 4, 11, 32, 39, 70, 100, 130, 160 ]]
Perianal wart characterization includes counting the number of identified warts, the diameter measurement of each identified wart in millimeters and the photographic imaging of each identified wart during the treatment phase and the follow-up phase of the study
Secondary Outcome Measures
- Assessment of HPV subtype identification change [Days 0, 4, 11, 32, 39, 70, 100 130, 160]
HPV subtyping will be performed on specimens collected from the anal canal.
- Assessment of Anal dysplasia cytologic grade change [Days 0, 4, 11, 32, 39, 70, 100, 130, 160]
Anal dysplasia cytologic specimen collection will take place during the treatment phase and the follow-up phase of the study
- Assessment of adverse effects during the treatment phase of the study assessed [Days 0, 4, 11, 32, 39, 70, 100, 130, 160]
Adverse effects experienced during the treatment phase of the study are recorded by the study participants in a symptoms log
Eligibility Criteria
Criteria
Inclusion Criteria:
-
≥18 years of age
-
Diagnosed with perianal condyloma by primary clinician
-
HIV-infected, may be on or off of antiretroviral therapy. Enrolment of subjects on HAART will be restricted to those individuals for whom an alternative regimen can reasonably be constructed in case of failure.
-
Negative reaction to intradermal test with ciprofloxacin (a fluoroquinolone antibiotic)
-
Any CD4 count will be considered appropriate for study
-
Blood WBC > 2.0x103/mm3 and absolute neutrophils count > 500
-
Blood hemoglobin > 10.0 g/dL
-
Blood platelet count > 50x103/mm3
-
Serum total bilirubin < 6.0 mg/dL (participants taking atazanavir-based ARV regimens may have elevated total bilirubin but are generally < 6)
-
Blood aspartate aminotransferase (AST) < 100 U/L (<2 ULN)
-
Blood alanine aminotransferase (ALT) < 130 U/L (<2 ULN)
-
Serum creatinine < 1.5 mg/dL
-
ECOG performance status < 3
-
If a subject is of reproductive potential he/she and her/his sexual partner MUST be willing and able to utilize highly effective methods of contraception (e.g., birth control pill, barrier methods with spermicide - as applicable) for the duration of the study including the study follow-up period.
-
Subjects must be willing to refrain from anal sex, douching and use of enemas prior to scheduled Pap smears
Exclusion Criteria:
-
Anal cancer (current or history of)
-
Inability to attend study visits
-
Participation in any other drug study
-
History of asthma
-
History of CHF and/or cardiac support for arrhythmia or on chronic cardiac medication or has other chronic or acute cardiac ailments (e.g., or abnormal EKG at Baseline)
-
History of organ transplantation or requiring chronic administration of immune suppressive drugs in the last 6 months
-
For women, neither pregnant nor lactating
-
In the opinion of the Primary Investigator, the subject may not be able to tolerate the study treatment regimen
-
Subjects who are currently using or have recently within past 3 months) been treated with immunomodulators (e.g., Interferon-α)
-
Subjects with active infections including sexually transmitted diseases (e.g., N. gonorrhea, C. trachomatis, H. ducreyi, T. pallidum)
-
History of allergic reaction to fluoroquinolone antibiotics (e.g., ciprofloxacin, ofloxacin)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Naval Medical Center San Diego | San Diego | California | United States | 92134-5000 |
| 2 | University of California San Francisco | San Francisco | California | United States | 94115 |
Sponsors and Collaborators
- CEL-SCI Corporation
- Ergomed Clinical Research Inc.
- United States Naval Medical Center, San Diego
Investigators
- Study Director: Eyal Talor, PhD, CEL-SCI Chief Scientific Officer
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- NMCSD2013.008_UCSF