PRGN-2012 + Bevacizumab for Respiratory Papillomatosis

SS
SM
Overseen ByScott M Norberg, D.O.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether combining two treatments, PRGN-2012 (a vaccine-based treatment) and bevacizumab (a drug that inhibits blood vessel growth), can help control recurrent respiratory papillomatosis (RRP). RRP is a rare condition that causes wart-like growths in the airway, making speaking or breathing difficult. The goal is to determine if these treatments can reduce the recurrence of these growths. It is suitable for adults with RRP who have undergone more than two surgeries to remove papillomas or have previously received PRGN-2012 or bevacizumab. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

Do I need to stop my current medications to join the trial?

The trial protocol does not specify if you need to stop taking your current medications. However, you cannot participate if you have taken certain investigational agents or systemic RRP therapies within 4 weeks before starting the study. It's best to discuss your current medications with the study team to ensure eligibility.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that using PRGN-2012 with bevacizumab appears promising for safety. Bevacizumab, previously used, is generally well-tolerated, with mild and manageable side effects in about 38% of patients. PRGN-2012, a vaccine-based treatment, has also been studied and found to be safe. In one study, more than half of the patients treated with PRGN-2012 experienced a complete response without major safety issues. Although using these treatments together is new, both have demonstrated acceptable safety in past research.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the combination of PRGN-2012 and Bevacizumab for respiratory papillomatosis because it offers a novel approach to tackling this challenging condition. Unlike traditional treatments, which often involve repeated surgeries to remove papillomas, PRGN-2012 is a therapeutic vaccine designed to stimulate the immune system to target and destroy the HPV-infected cells causing the papillomas. Bevacizumab, on the other hand, is an angiogenesis inhibitor that works by cutting off the blood supply to the papillomas, potentially reducing their growth. Together, these treatments might offer a more effective and less invasive option for patients who currently rely on surgical interventions.

What evidence suggests that this trial's treatments could be effective for respiratory papillomatosis?

Research has shown that PRGN-2012, a vaccine-based treatment, holds promise for treating recurrent respiratory papillomatosis (RRP). In studies, 83% of patients experienced a complete response, with their papillomas either significantly improving or disappearing. PRGN-2012 also reduced the need for surgeries in 86% of patients, helping to prevent the recurrence of papillomas. Bevacizumab, another treatment in this trial, has shown effectiveness for RRP with a response rate of about 71%. This drug works by affecting blood vessel growth, which can help stop the spread of papillomas. Participants in this trial will receive both PRGN-2012 and Bevacizumab together, aiming to control RRP and reduce the frequency of surgeries.12345

Who Is on the Research Team?

SM

Scott M Norberg, D.O.

Principal Investigator

National Cancer Institute (NCI)

Are You a Good Fit for This Trial?

This trial is for adults 18 and older with recurrent respiratory papillomatosis (RRP) who have needed at least two surgeries or certain treatments in the past year. Participants must be generally healthy, not pregnant or breastfeeding, able to use contraception, and free from serious heart problems, uncontrolled high blood pressure, recent major surgery, or severe allergies to study drugs.

Inclusion Criteria

Women breastfeeding or planning to breastfeed must discontinue breastfeeding from study treatment initiation
I have a confirmed diagnosis of RRP from a pathology report or biopsy.
I am 18 years old or older.
See 7 more

Exclusion Criteria

I have had serious heart or blood clot problems in the past year.
Known active alcohol or drug abuse
I have had major surgery involving tissue layers within the last 4 weeks.
See 17 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Treatment

Participants receive monotherapy with bevacizumab for 3 doses, followed by combination treatment with bevacizumab and PRGN-2012 for 2 doses, and PRGN-2012 alone for 2 doses over approximately 6 months

6 months
7 visits (in-person)

Follow-up

Participants are monitored for papilloma recurrence and safety, with assessments at 6, 12, 24, and 52 weeks, and every 3 months for an additional 2 years

3 years
4 visits (in-person) over 1 year, then contact every 3 months

Retreatment (if necessary)

Participants may receive a second course of treatment if RRP worsens during follow-up

What Are the Treatments Tested in This Trial?

Interventions

  • Bevacizumab
  • PRGN-2012

Trial Overview

The study tests a combination of PRGN-2012 (a vaccine-based treatment) and bevacizumab (a drug that blocks blood vessel growth), given by injection and IV over about six months. The goal is to see if using both together helps control RRP better than current approaches.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Arm 1Experimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

National Cancer Institute (NCI)

Lead Sponsor

Trials
14,080
Recruited
41,180,000+

Citations

PRGN-2012 gene therapy in adults with recurrent ...

PRGN-2012 treatment resulted in complete response in 51% of the patients treated and was safe.

Combination Bevacizumab and PRGN-2012 in Adults With ...

If their RRP gets worse during the follow-up period, they may be able to receive a second course of treatment using the same schedule....

HPV Genotype as a Predictor of Bevacizumab Treatment ...

The overall response rate (ORR) was 70.59%. Adverse events were observed in 38.24% of patients, Systemic bevacizumab is effective and well-tolerated in both ...

PRGN-2012 gene therapy in adults with recurrent ...

PRGN-2012 treatment resulted in complete response in 51% of the patients treated and was safe. Based on these positive pivotal study results, a ...

PRGN-2012 for Respiratory Papillomatosis

In studies, 83% of patients experienced a complete response, significantly improving their symptoms.