PEP-CMV in Recurrent MEdulloblastoma/Malignant Glioma

Malignant Glioma Clinical Trial

— PRiME  

Official title:

The PRiME Study: PEP-CMV in Recurrent MEdulloblastoma/Malignant Glioma

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03299309
• Other study ID #: Pro00079843
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: June 29, 2018
• Est. completion date: April 2025

Study information

• Verified date: May 2024
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary goal of this prospective clinical trial is to evaluate the safety of PEP-CMV in patients with recurrent medulloblastoma and malignant glioma. Patients with histologically-proven medulloblastoma or malignant glioma who had received prior therapy for their initial diagnosis and subsequently had tumor recurrence/progression may be enrolled any time after recurrence/progression regardless of prior adjuvant therapy. PEP-CMV is a vaccine comprised of Component A, a synthetic long peptide (SLP) of 26 amino acid residues from human pp65. In May 2021, enrollment on the study was temporarily suspended due to delays in vialing the PEP-CMV study vaccine.

Description:

Once a patient has enrolled onto this study, prior therapy will be terminated and patients will receive temozolomide 200 mg/m2/day x 5 days. If they are receiving bevacizumab at the time of enrollment, they will continue bevacizumab 10 mg/Kg every 14 days.

Patients who are ≥ 18 years of age will receive a tetanus (Td) booster at the time of enrollment. Immunotherapy begins with a Tetanus (Td) pre-conditioning vaccine delivered intradermally (i.d.) in the right groin at the site of the vaccine injection 6-24 hours prior to the first vaccine on day 21. The PEP-CMV vaccine will be administered as follows: PEP-CMV Component A mixed with Montanide ISA-51 (1:1 volume ratio) intradermally administered half in the RIGHT groin and half in the LEFT groin.

The first 3 PEP-CMV vaccines will occur every 2 weeks, then PEP-CMV vaccines will continue monthly (+/- 2 weeks) for no more than 10 years. Blood will be obtained for immune system monitoring.

In May 2021, enrollment on the study was temporarily suspended due to delays in vialing the PEP-CMV study vaccine.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: April 2025
• Est. primary completion date: April 27, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 3 Years to 35 Years

Eligibility

Inclusion Criteria:

1. Patients who are 3 - 35 years old

2. Histopathologically proven previous diagnosis of medulloblastoma or Grade III or IV glioma.

3. Radiology evidence of recurrent medulloblastoma (reMB) or recurrent Grade III and IV glioma. Patients will be considered for a biopsy or resection of the recurrent/progressive tumor at the discretion of the treating neurosurgeon and neuro-oncologist.

4. Brain MRI within one month prior to enrollment.

5. Received prior therapy for their initial diagnosis prior to recurrence/progression or who are unable to receive radiation therapy due to genetic disorders that put them at significant risk for radiation-induced secondary malignancies (i.e. Gorlin's syndrome or NF1 mutation).

6. Patients with neurological deficits should have deficits that are stable for a minimum of 2 weeks prior to registration.

7. Karnofsky Performance Status (KPS) of = 60% (KPS for > 10 years of age) or Lansky performance Score (LPS) of = 60 (LPS for = 10 years of age) assessed within 2 weeks prior to registration. Patients who are unable to walk because of paralysis but who are up in a wheel chair will be considered ambulatory for the purposes of the performance score.

8. Bone Marrow:

• ANC (Absolute neutrophil count) = 1000/µl (unsupported)*.

• Platelets = 100,000/µl (unsupported)*.

• Hemoglobin > 8 g/dL (may be supported).

9. Renal:

• Serum creatinine = upper limit of institutional normal.

10. Hepatic:

• Bilirubin = 1.5 times upper limit of normal for age.

• SGPT (ALT) = 3 times institutional upper limit of normal for age.

• SGOT (AST) = 3 times institutional upper limit of normal for age.

11. Patients of childbearing or child-fathering potential must be willing to use a medically acceptable form of birth control, which includes abstinence, while being treated on this study.

12. Signed informed consent according to institutional guidelines must be obtained prior to registration.

13. Any prior chemoradiotherapy is allowed.

Exclusion Criteria:

1. Pregnant or need to breast feed during the study period (Negative serum pregnancy test required).

2. Active infection requiring treatment or an unexplained febrile (> 101.5 degrees F) illness.

3. Known immunosuppressive disease or human immunodeficiency virus infection.

4. Patients with active renal, cardiac (congestive cardiac failure, myocardial infarction, myocarditis), or pulmonary disease.

5. Patients receiving concomitant immunosuppressive agents for medical condition.

6. Patients who need definitive radiotherapy for treatment of recurrent MB or recurrent Grade III or IV glioma.

7. Patients receiving any other investigational drug therapy.

8. Patients on corticosteroids > 0.1 mg/Kg/day (i.e. > the maximum dose of 4 mg/day).

9. Patients with any clinically significant unrelated systemic illness (serious infections or significant cardiac, pulmonary, hepatic or other organ dysfunction).

10. Patients with inability to return for follow-up visits or obtain follow-up studies required to assess toxicity to therapy.

Related Conditions & MeSH terms

• Brain Neoplasms
• Glioma
• Malignant Glioma
• Medulloblastoma
• Recurrence
• Recurrent Brain Tumor, Childhood
• Recurrent Medulloblastoma

Intervention

Drug:
• PEP-CMV
Patients receive temozolomide (TMZ) 200 mg/m2/day x 5 days. On day 20, patients will receive a Tetanus-diphtheria pre-conditioning vaccination with Td (tetanus, diphtheria toxoid, adsorbed). Immunotherapy begins the following day, on day 21, with injection of the PEP-CMV vaccine as follows: PEP-CMV Component A mixed with Montanide ISA-51 intradermally administered half in the RIGHT groin and half in the LEFT groin.

Locations

Country	Name	City	State
United States	Duke University Medical Center	Durham	North Carolina

Sponsors (3)

Lead Sponsor	Collaborator
Daniel Landi	Annias Immunotherapeutics, Inc., Pediatric Brain Tumor Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of patients with unacceptable toxicity	Evaluate the safety of PEP-CMV in pediatric patients with recurrent MB or recurrent Grade III/IV glioma	2 weeks after the 3rd PEP-CMV vaccine on the last enrolled patient
Secondary	Mean or median change from baseline at each follow-up assessment in ELISPOT (IFN-?)	Quantitate the immune response to the components of the PEP-CMV vaccine by ELISPOT	24 months
Secondary	Mean or median change from baseline at each follow-up assessment in ELISA (gB-KLH)	Quantitate the immune response to the components of the PEP-CMV vaccine by ELISA	24 months

External Links

•   Duke Cancer Institute
•   The Preston Robert Tisch Brain Tumor Center at Duke