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NCT Number: NCT06577532

Study of KRAS Neoantigen mRNA Vaccine (ABO2102) in Patients With KRAS -Mutated Solid Tumors

The purpose of this study is to evaluate the safety, immunogenicity, pharmacodynamics, as well as preliminary efficacy of KRAS neoantigen mRNA vaccine (ABO2102) alone and in combination with toripalimab (anti-PD-1 monoclonal antibody) among participants with KRAS-mutated advanced pancreatic cancer and other solid tumors. The trial includes dose escalation (Part I) and dose expansion(Part II) parts.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine

Shanghai, China

Location status: Recruiting

Location contact

Baiyong Shen

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥18 years of age at time of informed consent.
  • Participants with histologically and/ or cytologically confirmed advanced solid tumors (such as pancreatic ductal adenocarcinoma, non-small cell lung cancer, etc.), whose disease has progressed or being intolerant to relevant treatments during or following at least one line of systemic treatment; patients in the second stage include those who have experienced disease progression or intolerance to previous systemic treatments, as well as those who have not received systemic therapy but are deemed by the investigator to potentially benefit from the study treatment based on a comprehensive clinical assessment.
  • Harboring at least one of the targeted KRAS mutants.
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0~2.
  • Life expectancy of ≥12 weeks.
  • Sufficient organ function.

Exclusion criteria

  • Any other prior malignancy active within the previous 5 years, except for skin basal cell cancer that have been cured, superficial bladder cancer, or carcinoma in situ of the breast or cervix.
  • Received KRAS cancer vaccine before.
  • Immunosuppressants or other immunomodulatory drugs were required within 4 weeks before the first dose of study treatment. Physiological doses of systemic steroids or topical medications are allowed. Topical medications should not exceed the dose recommended in the package insert or have any systemic exposure signs; Or patients with other acquired or congenital immunodeficiency diseases, or a history of organ transplantation who need to use immunosuppressants or other immunomodulatory drugs.
  • History of severe allergies or known allergies to any active or inactive component of the study drug(s).
  • Uncontrolled systemic infection; active tuberculosis.
  • Severe cardiovascular diseases.
  • Has known symptomatic, untreated central nervous system metastases, or CNS metastases requiring continued treatment. Participants with asymptomatic brain metastases and who do not require treatment are eligible for enrolment.
  • Have active autoimmune and inflammatory diseases.
  • Have immediate hypersensitivity, a history of eczema or asthma uncontrolled by topical corticosteroids.
  • Have other serious medical conditions
  • A history of organ transplantation, bone marrow transplantation or hematopoietic stem cell transplantation.

Treatment and study plan

ABO2102

Drug

mRNA encoding mutant KRAS neoantigens, administrated intramuscularly

Toripalimab

Drug

Anti-PD-1 antibody, administered intravenously

Primary outcomes

  1. Part I: The incidence and nature of dose-limiting toxicity (DLT) for ABO2102 as monotherapy or in combination with toripalilmab.

    Time frame: 21 days after the first dose of study treatment

  2. Part I: The incidence and severity of treatment-emergent adverse events (TEAE)s.

    Time frame: from the first dose of study treatment to 30 days after the last dose of monotherapy or to 90 days after the last dose of the combination therapy.

  3. Part I: The incidence and severity of serious TEAEs (TESAE)s.

    Time frame: from the first dose of study treatment to 30 days after the last dose of monotherapy or to 90 days after the last dose of the combination therapy.

  4. Part I: The incidence and severity of TEAEs leading to interruption or early termination of study treatment.

    Time frame: from the first dose of study treatment to 30 days after the last dose of monotherapy or to 90 days after the last dose of the combination therapy.

  5. Part II: Overall Response Rate (ORR) per RECIST version 1.1.

    Time frame: from the first dose of study treatment to up to 2 years.

Study contacts

Contact information is provided by the study sponsor or research team.

Xinjing Wang

CONTACT

[email protected]

18817821319

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Collaborators

  • Suzhou Abogen Biosciences Co., Ltd.

Registry information

Official study title

A Clinical Study to Investigate Safety, Tolerability, Immunogenicity, and Preliminary Efficacy of mRNA Nanoparticles Encoding KRAS Neoantigens (ABO2102) in Participants With KRAS-mutated Advanced Pancreatic Cancer And Other Solid Tumors

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Aug 29, 2024
Registry last updated
May 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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