Status:
COMPLETED
HARE-40: HPV Anti-CD40 RNA vaccinE
Lead Sponsor:
University of Southampton
Collaborating Sponsors:
BioNTech SE
Conditions:
Human Papilloma Virus Related Carcinoma
Head and Neck Neoplasm
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
HARE-40 is a phase I/II vaccine dose escalation study with two different arms: Arm 1A will perform intrapatient dose escalation in patients with previously treated HPV16+ Head \& Neck Cancer using two...
Detailed Description
HARE-40 is a phase I/II vaccine dose escalation trial with two arms (Arm 1A and Arm 1B) in which we will test BNT113 as monotherapy. We will undertake a multi-centre phase I, open label trial in patie...
Eligibility Criteria
Inclusion
- Arm 1A:
- Previous HPV16+ head and neck squamous cell carcinoma.
- At least 12 months after completion of treatment.
- Within 5 years of treatment completion.
- Currently no clinical evidence of disease.
- ECOG performance status 0 or 1.
- Arm 1B:
- HPV16+ head and neck, cervical, anogenital and penile carcinoma patients with recurrent disease.
- Intention to treat is palliative.
- Patient willing to have repeated tumour biopsies and re-biopsy deemed safe and feasible clinically.
- Tissue samples available confirming HPV16+ disease to send to Central Laboratory.
Exclusion
- Patients unable to consent.
- Any patient who has been previously vaccinated in any Arm of the trial.
- \<18 years
- Systemic steroids (prednisolone \>10 mg/day or equivalent) or other drugs with a likely effect on immune competence are forbidden during the trial. The predictable need of their use will preclude the patient from trial entry. Replacement steroids for adrenal insufficiency/failure are allowed.
- Major surgery in the preceding three to four weeks, which the patient has not yet recovered from.
- Patients who are of high medical risk because of non-malignant systemic disease, as well as those with active uncontrolled infection.
- Patients with clinically relevant autoimmune disease will be excluded.
- Patients who are known to be allergic to any of the excipients or constituents of the vaccine
- Patients with any other condition which in the Investigator's opinion would not make the patient a good candidate for the clinical trial, such as concurrent congestive heart failure or prior history of New York Heart Association (NYHA) class III/IV cardiac disease.
- Current malignancies at other sites, with the exception of adequately treated basal or squamous cell carcinoma of the skin. Cancer survivors, who have undergone potentially curative therapy for a prior malignancy, have no evidence of that disease for five years and are deemed at low risk for recurrence, are eligible for the study.
- Patients who are serologically positive for or are known to suffer from Hepatitis B, C, Syphilis or HIV. Counselling will be offered to all patients prior to testing.
- Patients who have a positive pregnancy test or who are breast feeding.
- Fertile males or females who are unable or unwilling to use an effective method of birth control (eg. condom with spermicide, diaphragm with spermicide, birth control pills, injections, patches, intrauterine device, or intrauterine hormone-releasing system) during study treatment and until 28 days after patients finish the study treatment.
- Elevated Liver Function Tests - ALT \>3.0 x ULN, AST \>3.0 x ULN, Bilirubin \>3.0 x ULN.
- Any other investigational drug within 28 days or 5 half-lives depending on what gives the longer range before the first treatment of this study
Key Trial Info
Start Date :
April 11 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 24 2024
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT03418480
Start Date
April 11 2017
End Date
January 24 2024
Last Update
February 7 2024
Active Locations (2)
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1
Univeristy Hospitals Southampton NHS Foundation Trust
Southampton, Hampshire, United Kingdom, SO16 6YD
2
The Christie NHS Foundation Trust
Manchester, United Kingdom, M20 4BX