60 Participants NeededMy employer runs this trial

ITI-5000 Vaccine + Pembrolizumab for Breast Cancer

(VITAL-TNBC Trial)

Recruiting at 1 trial location
SL
Overseen ByScott L Wehage, M.S.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new cancer vaccine, ITI-5000, to determine if it can help the immune system attack triple-negative breast cancer (TNBC) cells. The vaccine trains the body to target specific proteins on these cancer cells. The study consists of two parts: the first tests different doses of the vaccine alone, and the second combines the optimal dose with an existing immunotherapy drug, pembrolizumab. Ideal participants have completed standard treatments for early-stage TNBC within the last 36 months and have no major heart issues or active autoimmune diseases. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this innovative therapy.

Do I have to stop taking my current medications for the trial?

The trial protocol does not specify if you need to stop taking your current medications. However, you cannot use alternative therapies during the study and must avoid certain vaccines close to the trial period.

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

Research has shown that ITI-5000, an experimental cancer vaccine, is being tested for safety and effectiveness in working with the immune system. Although specific safety details for ITI-5000 are not yet available, it is based on a method similar to approved mRNA vaccines, which are generally well-tolerated.

In animal studies, ITI-5000 demonstrated greater effectiveness without additional safety concerns, suggesting potential safety for humans. However, ongoing trials are needed to provide more information.

Pembrolizumab, used with ITI-5000, is already approved for treating certain breast cancers and has a known safety profile, with common side effects like tiredness and headache. Its use with a personalized mRNA vaccine in other studies has shown promising results without unexpected safety issues.12345

Why are researchers excited about this trial's treatments?

Unlike the standard treatments for breast cancer, which often include chemotherapy, hormone therapy, and targeted therapies, the ITI-5000 mRNA vaccine offers a novel approach by using mRNA technology to stimulate the body's immune system to target cancer cells. Researchers are excited about this treatment because it harnesses the body’s natural defenses and could potentially provide a more precise attack on cancer cells with fewer side effects. Additionally, when combined with pembrolizumab, an immune checkpoint inhibitor, this treatment aims to enhance the immune response even further, offering a promising new avenue for patients who might not respond to conventional therapies.

What evidence suggests that this trial's treatments could be effective for triple-negative breast cancer?

Research has shown that the ITI-5000 vaccine may help fight triple-negative breast cancer (TNBC) by training the immune system to attack cancer cells with specific proteins. Studies have found that the vaccine can generate strong immune responses, with many patients experiencing significant tumor reduction and longer survival. In this trial, some participants will receive ITI-5000 as monotherapy, while others will receive it in combination with pembrolizumab, a well-known cancer drug. This combination has demonstrated improvements in keeping patients cancer-free. In some cases, similar vaccine and drug combinations have led to a 49% decrease in cancer recurrence or mortality. This suggests that ITI-5000, especially when combined with pembrolizumab, might effectively reduce cancer recurrence in TNBC patients.12367

Are You a Good Fit for This Trial?

This trial is for adults (18+) with stage II or III triple-negative breast cancer who have finished all standard treatments within the past 3 years. Participants must be in good overall health, not pregnant or breastfeeding, and able to follow study procedures. Certain heart problems, autoimmune diseases needing treatment, recent major illness, or allergies to vaccine ingredients exclude participation.

Inclusion Criteria

I can understand the study and sign a consent form.
Able to attend required study visits and follow-up
I am 18 years old or older.
See 9 more

Exclusion Criteria

Significant medical illness, underlying health condition, or abnormal laboratory finding increasing risk
Positive serum pregnancy test at screening or positive urine test at baseline
Concurrent participation in any other interventional clinical trial
See 18 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment Part A

Participants receive ITI-5000 alone at one of two dose levels (1 µg or 10 µg) every 28 days for 3 doses total to find the safest dose.

12 weeks
3 visits (in-person)

Treatment Part B

Participants receive ITI-5000 at the best dose identified in Part A, combined with pembrolizumab every 21 days for 3 doses total.

9 weeks
3 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment.

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • ITI-5000 mRNA Vaccine
  • Pembrolizumab

Trial Overview

The study tests a new mRNA vaccine called ITI-5000 given alone at different doses (Part A) or combined with pembrolizumab immunotherapy (Part B). The goal is to find a safe dose and see how well the combination works after standard TNBC treatment.

How Is the Trial Designed?

5

Treatment groups

Experimental Treatment

Group I: Part B ITI-5000 and Pembrolizumab+CapecitabineExperimental Treatment3 Interventions
Group II: Part B ITI-5000 and Pembrolizumab + OlaparibExperimental Treatment3 Interventions
Group III: Part A, Cohort 3 ITI-5000 Monotherapy ExpansionExperimental Treatment1 Intervention
Group IV: Part A, Cohort 2 ITI-5000 10 µg MonotherapyExperimental Treatment1 Intervention
Group V: Part A, Cohort 1 ITI-5000 1 µg MonotherapyExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Immunomic Therapeutics, Inc.

Lead Sponsor

Trials
9
Recruited
480+

Citations

First-in-human, Phase 1 Study of a Self-amplifying RNA ...

This study tests an investigational cancer vaccine called ITI-5000 in people who have completed standard treatment for early-stage ...

Advancements in breast cancer mRNA vaccines

The vaccine demonstrated significant anti-tumour effects in both prophylactic and therapeutic experiments, effectively suppressing tumour growth and prolonging ...

ITI Announces FDA Clearance of IND Application for a UNITE

TNBC represents approximately 15%–20% of breast cancer diagnoses and remains associated with poorer outcomes and fewer targeted treatment ...

ITI-5000 TNBC Vaccine + Pembrolizumab and ITI ... - ICH GCP

This study tests an investigational cancer vaccine called ITI-5000 in people who have completed standard treatment for early-stage ...

A recent study showed that adding a personalized mRNA ...

The combination demonstrated a statistically significant and clinically meaningful improvement in the primary endpoint of recurrence-free ...

6.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/41708868/

Individualized mRNA vaccines evoke durable T cell ...

Triple-negative breast cancer (TNBC) is frequently associated with metastatic relapse, even at an early stage 1 . Here we assessed an individualized ...

Immunomic Therapeutics Announces FDA Clearance of ...

"Preclinical data have demonstrated enhanced efficacy in animal models without additional safety concerns. The FDA's clearance of our IND ...