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Phase 1 Study of a Self-amplifying RNA Vaccine (ITI-5000) in Stage 2-3 Triple Negative Breast Cancer (VITAL-TNBC)

2026년 9월 8일 업데이트: Immunomic Therapeutics, Inc.

A Phase 1, Multicenter, Open-label, First-in-Human Study of ITI-5000 (Self-Amplifying RNA Vaccine) Alone and in Combination With Standard of Care Adjuvant Therapy in Participants With Stage II-III Triple-Negative Breast Cancer (TNBC)

This study tests an investigational cancer vaccine called ITI-5000 in people who have completed standard treatment for early-stage triple-negative breast cancer (TNBC).

ITI-5000 is a self-amplifying RNA (saRNA) vaccine that instructs the immune system to recognize and attack cancer cells expressing two proteins found on TNBC cells-HERV-K and CT83-fused with a molecule called LAMP-1 that helps the immune system respond more strongly. The vaccine is delivered inside lipid nanoparticles (LNPs), similar to other approved mRNA vaccines.

The study has two parts:

  • Part A: Participants receive ITI-5000 alone at one of two dose levels (1 µg or 10 µg), given as an injection into the upper arm muscle every 28 days for 3 doses total. The goal is to find the safest dose.
  • Part B: Participants receive ITI-5000 at the best dose identified in Part A, combined with the following approved immunotherapy drugs pembrolizumab (Keytruda) and either olaparib or capecitabine.

연구 개요

상세 설명

This will be a phase 1, FIH, multicenter, open-label, two-part, ascending dose study to evaluate the safety, tolerability, and immune response of the ITI-5000 vaccine in adult participants with TNBC (stage 2-3). The study will be divided into 2 parts: in Part A, participants will receive the ITI-5000 vaccine as a single agent in the post-adjuvant setting, and in Part B, participants will receive the ITI-5000 vaccine in combination with standard of care adjuvant therapy.

Part A will be divided into 2 dose level cohorts - Cohort 1A conducted at the dose of 1 μg (low dose) per vaccination and Cohort 2A conducted at the dose of 10 μg (high dose) per vaccination. In Part A, three vaccinations of ITI-5000 will be administered with a 28-day interval.

The first 3-6 participants will be enrolled sequentially, with the first participant designated as a sentinel participant who will be monitored for 28 days after receiving the first ITI-5000 vaccination before subsequent participants are enrolled. If 0/3 participants experience a DLT, Cohort 2A may proceed. If 1/3 of the participants experience a DLT, the cohort will expand to include 3 additional participants (total of 6). If ≥2/6 participants experience a DLT, the dose will be considered not tolerable, and the cohort will be stopped.

At the conclusion of each cohort, the safety review committee (SRC) will review safety signals and determine a rationale for dose escalation, de-escalation, or potential intermediate doses to be evaluated. The SRC will also determine the dose to be evaluated in Cohort 3A and Part B.

The MTD will be evaluated in Cohort 3A which will enroll up to 15 participants who did not achieve pathological complete response (pCR) following neoadjuvant therapy. This expansion will allow further assessment of safety and immunogenicity in a participant population that is at high risk of disease recurrence.

Part B will evaluate the MTD of ITI-5000 in combination with standard of care (SOC) adjuvant therapy among participants who did not achieve a pathological complete response (pCR) following neoadjuvant therapy.

A safety lead-in group comprising 3 participants will be enrolled at the beginning of Cohort 1B and 2B to assess the safety of the combination treatment. Unlike Part A, no sentinel participant will be required, as the safety of ITI-5000 alone will already have been established in Part A. The safety lead-in will provide an early evaluation of the tolerability of the combination regimen before enrolling additional participants.

Cohort 1B will enroll up to 20 participants with BRCA1/2 mutation who did not achieve pathological complete response (pCR) following neoadjuvant therapy. Three doses of ITI-5000 will be administered in the adjuvant setting with a 21-day interval in combination with standard of care (pembrolizumab 200 mg Q3 weeks or 400 mg Q6 weeks and olaparib as per FDA approved label and currently accepted guidelines).

Cohort 2B will enroll up to 20 participants with wild-type BRCA1/2 who did not achieve pCR following neoadjuvant therapy. Three doses of ITI-5000 will be administered in the adjuvant setting with a 21-day interval in combination with standard of care (pembrolizumab 200 mg Q3 weeks or 400 mg Q6 weeks and capecitabine as per FDA approved label and currently accepted guidelines).

Following SRC review of the safety lead-in participants, an expansion cohort of up to 17 additional participants will be enrolled in both Cohorts 1B and 2B, bringing Part B to a total of up to 40 participants (up to 20 participants per cohort).

After all Part B participants have completed the Follow-up #1 visit, the SRC will meet to guide further clinical development of ITI-5000. The final analysis will take place after the end of the study.

In both Part A and Part B, participants will undergo 3 main study periods: a screening period, a treatment period (also named study vaccination period) with 3 study visits during which each participant will receive a total of 3 ITI-5000 vaccinations: 28 days

연구 유형

중재적

등록 (추정된)

60

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Michigan
      • Grand Rapids, Michigan, 미국, 49546
    • Tennessee
      • Nashville, Tennessee, 미국, 37203
        • 모병
        • Sarah Cannon Research Institute
        • 연락하다:
        • 수석 연구원:
          • Sarah Premji, MD

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  1. Applicable to Part A only. Participants must have completed adjuvant pembrolizumab if they were receiving it before enrolling in the study.
  2. Applicable to Cohort 3A and Part B only. Participant must have received neoadjuvant chemotherapy with pembrolizumab, then undergone definitive surgery. At the time of surgery, participant must not have achieved pCR.
  3. Applicable to Part B only. Participant is currently receiving or is planned to receive standard of care adjuvant therapy, including pembrolizumab in combination with capecitabine or olaparib in accordance with the FDA-approved label, with ≥3 cycles remaining if receiving 200mg Q3W or ≥2 cycles remaining if receiving 400 mg Q6W at the time of first ITI-5000 dose.
  4. Adults aged 18 years or over.
  5. Participants provided a signed and dated ICF.
  6. Participant agrees not to receive any routine vaccinations until at least 30 days after receiving the last study vaccine.
  7. TNBC diagnosed as pathologic stage 2-3 according to American Joint Committee on Cancer (AJCC) and confirmed by histological examination, e.g., negative for HER2 as defined by ASCO CAP 2023 guidelines. ER and PgR receptor negative by immunohistochemistry. Participants with BRCA mutations will be allowed.

    a. Concurrent endocrine therapy (e.g., tamoxifen, aromatase inhibitors, ovarian suppression) is not permitted during study participation. Concurrent CDK4/6 inhibitors (ribociclib/abemaciclib) are not allowed.

  8. Applicable to Part A only. Participants with more than 4 weeks since last active therapy (chemotherapy, radiation therapy, or surgery) and 36 months or less following definitive surgery, based on the period of highest risk for recurrence in participants with stages 2-3 TNBC.
  9. Applicable to Part A only. Participants completed all planned previous cancer treatment (e.g., chemotherapy, radiation, therapy, surgery).
  10. Participant's ECOG performance status is 0 or 1.
  11. Participant had no significant ischemic heart disease or myocardial infarction within 3 months before vaccination #1 and has adequate cardiac function during eligibility evaluation, as evidenced by QTc of ≤470 msec for females or ≤450 msec for males assessed by the Fridericia method (QTcF) and evidenced by the average of measurements from triplicate ECGs at the screening visit.

    a. The eligibility of participants with ventricular pacemakers for whom the QT interval may not be accurately measurable will be determined on a case-by-case basis by the sponsor in consultation with the medical monitor.

  12. Participant has an adequate organ function, as evidenced by the following tests conducted within 7 days before enrollment:

    i. Hematology examination (excluding blood transfusion or use of hematopoietic stimulating agents for correction):

1. Hemoglobin ≥8.0 g/L 2. Absolute neutrophil count (ANC) ≥1.0 × 109/L 3. Platelet count ≥100 × 109/L ii. Serum biochemistry examination (excluding recent blood transfusion or albumin administration):

1. Alanine aminotransferase and AST ≤1.5 times the ULN 2. Alkaline phosphatase ≤2.5 ULN 3. Total bilirubin ≤ 1.5 ULN 4. Serum creatinine ≤1.5 ULN, with creatinine clearance ≥ 50 mL/min (calculated using the Cockcroft-Gault formula) 13. Women of childbearing potential have a negative serum pregnancy test within 3 days before vaccination #1, and they and their partners agree to use highly effective methods of contraception during the study and for 6 months after the last administration of the study drug.

a. NOTE: A woman is considered of non-childbearing potential if she has had a documented bilateral oophorectomy, tubal ligation, or hysterectomy, or if she is postmenopausal, defined as ≥12 months of spontaneous amenorrhea without an alternative medical cause (with serum FSH confirmation if <55 years old). 14. Participant is able to attend the required study visits and follow-up as required by this protocol.

15. Participant is able to understand and provide a signed informed consent that fulfills the relevant IRB or IEC guidelines prior to study registration.

16. Participant agrees not to use alternative therapies from the time of informed consent through 30 days following vaccination #3. Participants may be asked to complete a "wash out" period before vaccination #1 at the principal investigator's discretion to ensure the absence of all alternative therapies.

NOTE: "Alternative therapies" refer to non-prescription or non-standard medical interventions used with the intent to treat or prevent cancer or its symptoms, including but not limited to herbal remedies, high-dose dietary supplements marketed for therapeutic benefit, homeopathic preparations, or naturopathic treatments. Routine vitamins, minerals, or supportive care measures not expected to affect immune function may be continued at the investigator's discretion.

Exclusion Criteria:

  1. Applicable to Part B only. Participant discontinued prior treatment with an ICI due to irAEs.
  2. Participant underwent major surgery within 4 weeks before the planned day of vaccination #1 or received any other investigational drug or device within 4 weeks or 5 half-lives of that agent (whichever is shorter) before the planned day of Vaccination #1.

    i. Applicable to Part A only. Participant received cancer-directed therapy (chemotherapy, radiotherapy, biologic or immunotherapy, etc.) within 4 weeks or 5 half-lives of that agent (whichever is shorter) before the planned day of Vaccination #1. ii. Applicable to Part B only. Participants who received any PD-1 or PD-L1 inhibitor other than pembrolizumab will be excluded unless they have completed a washout period of ≥ 4 weeks or 5 half-lives of that agent (whichever is shorter) before Vaccination #1.

  3. Participant has toxicities due to prior immunotherapy. For the participant to be eligible, these toxicities must either have returned to ≤ Grade 1 or baseline or been deemed irreversible and in the opinion of the investigator not worsened by immunotherapy (e.g., ICI-endocrinopathies). Participants with any cardiac toxicities (regardless of the grade, etc.) will be excluded.
  4. Participant has toxicities due to prior chemotherapy that have not been resolved or considered stable and clinically manageable (e.g., neuropathies). Participants with any cardiac toxicities will be excluded.
  5. Participant has a significant medical illness, underlying health condition, or abnormal laboratory finding that, in the investigator's opinion, would increase the risk of participating in the study.
  6. Participants with an active autoimmune disease requiring immunosuppressive treatment within the last year (excluding irAEs), such as chronic prolonged systemic corticosteroid use (defined as corticosteroid use lasting one month or more).
  7. Female participants who are trying to conceive, are pregnant, or lactating.
  8. A positive serum pregnancy test at screening and/ or a positive human chorionic gonadotropin (hCG) urine test at baseline in women of childbearing potential.
  9. Participant concurrently participates in any other interventional clinical trial.
  10. Participant has known allergies to any of the components of the study vaccine.
  11. Participant has a history of anaphylaxis requiring medical intervention (including severe reactions to other mRNA vaccines, such as those against SARS-COV-2, etc.).
  12. Participant has a history of stroke, transient ischemic attack, unstable angina, or myocardial infarction within 3 months prior to the first dose of study treatment.
  13. Participant has a history of myocarditis or pericarditis.
  14. Participant has symptomatic congestive heart failure according to New York Heart Association (NYHA) classification, Class III or IV (per NYHA Classification), clinically significant cardiac arrhythmia, or a known left ventricular ejection fraction <45%.
  15. Participant has a history of risk factors for torsade de pointes (e.g., heart failure, hypokalemia, family history of long QT syndrome) or requires the use during study participation of concomitant medications known or suspected to prolong the QT/QTc interval, with the exception of drugs with low risk of QT/QTc prolongation that are used as standard premedication (e.g., diphenhydramine, famotidine, ondansetron).
  16. Participant received an mRNA or a live virus vaccine within 28 days of the planned vaccination #1. Flu and COVID vaccinations/boosters are also prohibited within 28 days before the planned day of vaccination #1. Vaccines that do not contain live virus are permitted.
  17. Participant has prior malignancy, except for the following:

    i. adequately treated basal-cell or squamous-cell skin cancer, ii. in situ cervical cancer, iii. any other cancer from which the participant has been disease-free for at least 3 years.

  18. Participant has a history of organ transplant requiring immunosuppression. Participants with unstable human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) are not eligible.

    a. Stable and well controlled HIV/AIDS participants on retroviral therapy, defined as those with no dose change within 4 weeks before the planned day of vaccination #1 and no anticipated dose change, are eligible.

  19. Participant with known active hepatitis B or C are not eligible. Active hepatitis B is defined as a known positive hepatitis B surface antigen (HBsAg) result. Active hepatitis C is defined by a known positive hepatitis C antibody result and known quantitative hepatitis C virus RNA results greater than the lower limits of detection of the assay.

    a. Participants with a history of infection with hepatitis B virus or HCV may enroll if the viral load is undetectable per quantitative polymerase chain reaction (PCR) and/or nucleic acid testing.

  20. Participant was assessed by the investigator as being unable or unwilling to comply with the requirements of the treatment schedule and study procedures for any reason.
  21. Participant has a contraindication to IM injections or blood draws.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Part A, Cohort 1 ITI-5000 1 µg Monotherapy
Participants receive ITI-5000 1 µg as an intramuscular injection every 28 days for 3 doses.
Participants receive ITI-5000. Cohort 1 will receive 1 ug of vaccine
Participants receive ITI-5000. Cohort 2 will receive 10 ug of vaccine
실험적: Part A, Cohort 2 ITI-5000 10 µg Monotherapy
Participants receive ITI-5000 10 µg as an intramuscular injection every 28 days for 3 doses.
Participants receive ITI-5000. Cohort 1 will receive 1 ug of vaccine
Participants receive ITI-5000. Cohort 2 will receive 10 ug of vaccine
실험적: Part B ITI-5000 and Pembrolizumab + Olaparib
Participants receive ITI-5000 at the dose determined in Part A as an injection every 21 days for 3 doses. Participants will also receive pembrolizumab 200 mg or 400 mg per FDA-approved package insert plus Olaparib.
Participants will receive ITI-5000 as an intramuscular injection every 21 days for 3 doses. Participants will also receive pembrolizumab as per the FDA-approved package insert.
Participants will receive Olaparib in combination with Pembrolizumab and ITI-5000
Participants receive ITI-5000 Maximum Tolerated Dose (MTD)
실험적: Part A, Cohort 3 ITI-5000 Monotherapy Expansion
Participants receive ITI-5000 Maximum Tolerated Dose (MTD) as an intramuscular injection every 28 days for three doses
Participants receive ITI-5000 Maximum Tolerated Dose (MTD)
실험적: Part B ITI-5000 and Pembrolizumab+Capecitabine
Participants receive ITI-5000 at the dose determined in Part A as an injection every 21 days for three doses. Participants also receive Pembrolizumab 200 mg or 400 mg per FDA-approved package insert plus Capecitabine
Participants will receive ITI-5000 as an intramuscular injection every 21 days for 3 doses. Participants will also receive pembrolizumab as per the FDA-approved package insert.
Participants receive ITI-5000 Maximum Tolerated Dose (MTD)
Participants will receive Capecitabine in combination with Pembrolizumab and ITI-5000

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Incidence of Dose-Limiting Toxicities as Assessed by CTCAE v5.0
기간: 21-28 days after the first vaccination
21-28 days after the first vaccination

2차 결과 측정

결과 측정
기간
Incidence and severity of TEAEs, SAEs, treatment-related TEAEs, AESIs, and clinically significant abnormalities in laboratory parameters, vital signs, and ECGs
기간: From first dose through end of safety follow-up
From first dose through end of safety follow-up

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 7월 14일

기본 완료 (추정된)

2028년 2월 1일

연구 완료 (추정된)

2028년 8월 1일

연구 등록 날짜

최초 제출

2026년 6월 11일

QC 기준을 충족하는 최초 제출

2026년 6월 11일

처음 게시됨 (실제)

2026년 6월 17일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 8일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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