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PHASE 1 TRIAL OF Lm-LLO-TT AND GEMCITABINE IN UNRESECTABLE PANCREATIC DUCTAL ADENOCARCINOMA

14 settembre 2026 aggiornato da: Loki Therapeutics, Inc.

PHASE 1, OPEN-LABEL, FIRST-IN-HUMAN TRIAL OF INTRAPERITONEA L Lm-LLO-TT AND GEMCITABINE IN PARTICIPANTS WITH UNRESECTABLE PANCREATIC DUCTAL ADENOCARCINOMA

ClinicalTrials.gov Brief Summary

This Phase 1, open-label, first-in-human study is designed to evaluate the safety, tolerability, and recommended dose of intraperitoneal (IP) administration of Lm-LLO-TT in combination with low-dose gemcitabine in adults with previously treated, unresectable or metastatic pancreatic ductal adenocarcinoma (PDAC). Up to 18 participants will be enrolled.

Lm-LLO-TT is a live attenuated Listeria monocytogenes-based immunotherapy engineered to express a tetanus toxoid antigen. The study will assess the safety of administering Lm-LLO-TT directly into the peritoneal cavity and characterize its use in combination with low-dose gemcitabine.

Eligible participants will receive a tetanus toxoid booster vaccination during screening and undergo placement of an intraperitoneal access port before treatment. Participants will receive a single loading dose of Lm-LLO-TT followed by five cycles of low-dose gemcitabine and low-dose Lm-LLO-TT administered over approximately 17 days. Participants will be monitored for adverse events, laboratory abnormalities, dose-limiting toxicities, and disease outcomes throughout the study.

The primary objective is to assess safety and tolerability and to determine the maximum tolerated dose and recommended dose for future clinical studies. Secondary objectives include evaluation of anti-tumor activity. Exploratory objectives include assessment of immune biomarkers, changes in pancreatic cancer-related symptoms, and changes in pain medication use.

Participants will undergo tumor imaging assessments following treatment and during follow-up. A post-treatment tumor biopsy will be required for the first 10 enrolled participants and optional for subsequent participants. Participants will be followed for safety, disease status, and survival for up to 6 months after treatment initiation.

Panoramica dello studio

Descrizione dettagliata

This is a Phase 1, open-label, first-in-human, dose-escalation study designed to evaluate the safety, tolerability, maximum tolerated dose (MTD), and recommended Phase 2 dose (RP2D) of intraperitoneal (IP) administration of Lm-LLO-TT in combination with low-dose gemcitabine in participants with previously treated unresectable or metastatic pancreatic ductal adenocarcinoma (PDAC). Up to 18 participants will be enrolled. The study will use a Bayesian Optimal Interval (BOIN) dose-escalation design to identify the MTD and RP2D of Lm-LLO-TT for future clinical development.

PDAC is associated with poor clinical outcomes and limited treatment options in the advanced disease setting. Lm-LLO-TT is a live attenuated Listeria monocytogenes-based immunotherapy engineered to express a tetanus toxoid (TT) antigen linked to listeriolysin O (LLO). This study will evaluate the safety and biologic activity of administering Lm-LLO-TT directly into the peritoneal cavity in combination with low-dose gemcitabine.

Eligible participants are adults with histologically confirmed PDAC and measurable disease according to RECIST version 1.1 who have received at least one prior systemic treatment regimen for unresectable or metastatic disease or have a contraindication to standard therapies. Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2, adequate organ function, and a life expectancy greater than 3 months.

During screening, participants will undergo tetanus toxoid immunity testing. All participants will receive a tetanus toxoid booster vaccination before treatment initiation. Tetanus antibody titers will be evaluated before and after the booster vaccination, and evidence of an immune response to tetanus toxoid is required for enrollment. Participants will also undergo placement of an intraperitoneal access port before the first administration of study treatment.

Treatment begins with a single escalating loading dose of Lm-LLO-TT administered intraperitoneally on Day 1. Beginning on Day 2, participants will receive low-dose intraperitoneal gemcitabine followed the next day by low-dose intraperitoneal Lm-LLO-TT. This alternating schedule will be repeated for a total of five gemcitabine/Lm-LLO-TT treatment cycles over approximately 17 days.

The dose-escalation component evaluates escalating loading doses of Lm-LLO-TT while maintaining fixed doses of low-dose gemcitabine and low-dose Lm-LLO-TT. Participants will be enrolled sequentially into dose cohorts, and safety data including dose-limiting toxicities (DLTs) will be reviewed throughout the study. Escalation and de-escalation decisions will follow the protocol-defined BOIN design rules.

The primary objective of the study is to evaluate the safety and tolerability of intraperitoneal Lm-LLO-TT administered in combination with low-dose gemcitabine and to determine the MTD and RP2D. Safety evaluations include adverse event monitoring, physical examinations, vital signs, clinical laboratory assessments, electrocardiograms, and assessment of DLTs.

Secondary objectives include evaluation of preliminary anti-tumor activity. Tumor response will be assessed according to RECIST version 1.1 criteria. Secondary endpoints include objective response rate, disease control rate, and progression-free survival.

Exploratory objectives include assessment of pharmacodynamic and immune biomarkers associated with treatment. Blood samples will be collected for evaluation of circulating biomarkers, including circulating tumor DNA and markers associated with immune responses and tumor microenvironment modulation. Tumor tissue obtained during post-treatment biopsy procedures will be evaluated for immune cell infiltration, tetanus toxoid expression, and other tumor microenvironment biomarkers.

The first 10 enrolled participants will undergo a mandatory post-treatment tumor biopsy approximately 20 to 30 days following completion of treatment. Post-treatment biopsy will be optional for participants enrolled thereafter. Imaging assessments of the chest, abdomen, and pelvis will be performed at approximately Day 20 to 30 following treatment and repeated at approximately 4 and 6 months after treatment initiation.

Additional exploratory assessments will evaluate changes in pancreatic cancer-related symptoms, including pain, nausea, vomiting, and fatigue, as well as changes in concomitant pain medication use among participants who report pain at baseline.

Participants will be monitored for bacterial shedding through urine and fecal sample collection during the treatment and follow-up periods. Participants will also be monitored for safety events of special interest, including infection-related events associated with administration of live attenuated bacterial therapy.

Following completion of treatment, participants will enter a follow-up period that includes safety evaluations, disease assessments, laboratory testing, biomarker assessments, and survival follow-up. Participants will be followed for up to 6 months after initiation of study treatment.

Data generated from this study will be used to characterize the safety profile, determine the recommended dose for future studies, evaluate preliminary anti-tumor activity, and inform the further clinical development of intraperitoneal Lm-LLO-TT in combination with low-dose gemcitabine for the treatment of advanced pancreatic ductal adenocarcinoma.

Tipo di studio

Interventistico

Iscrizione (Stimato)

18

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • New York
      • The Bronx, New York, Stati Uniti, 10461
        • Einstein College of Medicine/Montefiore Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

Able and willing to provide written informed consent. Adults aged 18 years or older. Histologically confirmed pancreatic ductal adenocarcinoma (PDAC) with measurable disease per RECIST v1.1.

Previously treated with at least one line of chemotherapy for metastatic or unresectable disease, including a fluoropyrimidine-based or gemcitabine-based regimen, or have a contraindication to these therapies.

No radiation therapy, targeted therapy, or chemotherapy within 14 days prior to first study treatment; no immunotherapy or biologic therapy within 28 days prior to first study treatment.

Recovery to ≤ Grade 2 from clinically significant toxicities of prior therapy. ECOG Performance Status 0-2. Estimated life expectancy greater than 3 months. Adequate organ function, including adequate hematologic, hepatic, and renal function.

Participants with treated brain metastases may be enrolled if clinically stable for at least 1 month.

Willing to comply with study procedures and contraceptive requirements. Participants with HIV may be enrolled if receiving antiretroviral therapy and CD4 count is >400 cells/µL.

Participants with hepatitis B may be enrolled if viral load is undetectable and appropriately treated; participants with hepatitis C may be enrolled following curative treatment.

Demonstrated tetanus toxoid (TT) immune responsiveness, either at baseline or following administration of a tetanus toxoid booster during screening.

Exclusion Criteria:

  • History of chronic comorbidities that would significantly limit participation in the study, including severe heart failure (NYHA Class III-IV), end-stage renal disease, substance dependence, or inadequate venous access, as determined by the investigator.

Candidate for curative-intent surgical resection.

Surgery within 2 weeks prior to first study treatment.

Evidence of hepatic cirrhosis or clinically/radiographically significant ascites.

Blood transfusion within 14 days prior to study treatment or requirement for frequent blood transfusions (>2 per month).

Treatment with systemically active corticosteroids within 28 days before study treatment (except low-dose dexamethasone ≤2 mg/day or prednisone ≤10 mg/day).

Systemic antibiotic therapy within 14 days prior to first dose of Lm-LLO-TT.

Receipt of another investigational product or vaccine within 28 days prior to first study treatment.

Receipt of any vaccine other than the protocol-required tetanus toxoid booster within 4 weeks before study treatment or during the initial DLT evaluation period.

Major surgery, significant traumatic injury, unhealed surgical wounds, or planned surgery requiring general anesthesia within 28 days before study treatment.

Active, uncontrolled HIV, hepatitis B, hepatitis C, or HTLV-1 infection, or CD4 count <400 cells/µL.

Presence of implanted prosthetic devices, including orthopedic prostheses, pacemakers, or prosthetic heart valves.

Chronic immunosuppressive therapy for autoimmune or rheumatologic conditions.

Pregnant or breastfeeding individuals.

Active uncontrolled bacterial infection requiring intravenous antibiotics, fever >38.1°C, or unexplained fever within 7 days before Day 1.

History of Guillain-Barré syndrome within 6 weeks of a previous tetanus toxoid vaccination or prior Arthus-type hypersensitivity reaction to tetanus vaccine.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Dose elevata
Lm-LLO-TT is a live attenuated Listeria monocytogenes-based immunotherapy expressing tetanus toxoid and listeriolysin O, developed to stimulate tumor-directed immune responses through activation of tetanus-specific memory T cells.
Sperimentale: Low dose
Lm-LLO-TT is a live attenuated Listeria monocytogenes-based immunotherapy expressing tetanus toxoid and listeriolysin O, developed to stimulate tumor-directed immune responses through activation of tetanus-specific memory T cells.
Sperimentale: Middle dose
Lm-LLO-TT is a live attenuated Listeria monocytogenes-based immunotherapy expressing tetanus toxoid and listeriolysin O, developed to stimulate tumor-directed immune responses through activation of tetanus-specific memory T cells.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Safety and tolerability
Lasso di tempo: Day 1 to Day 45
Incidence of dose-limiting toxicities (DLTs) and treatment-emergent adverse events to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of intraperitoneal Lm-LLO-TT in combination with low-dose gemcitabine
Day 1 to Day 45

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate
Lasso di tempo: Up to 6 months
Percentage of participants with complete response or partial response as assessed by RECIST v1.1.
Up to 6 months
Disease Control Rate (DCR)
Lasso di tempo: Day 1 to 6 months
Percentage of participants with complete response, partial response, or stable disease as assessed by RECIST v1.1.
Day 1 to 6 months
Progression-Free Survival (PFS)
Lasso di tempo: Day 1 to 6 months
Time from first study treatment to documented disease progression or death.
Day 1 to 6 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 ottobre 2026

Completamento primario (Stimato)

15 ottobre 2028

Completamento dello studio (Stimato)

30 gennaio 2029

Date di iscrizione allo studio

Primo inviato

14 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 settembre 2026

Primo Inserito (Effettivo)

18 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data (IPD) collected during this study, including de-identified participant-level data and supporting study documents, will not be made available to other researchers. The study is an early-phase, first-in-human clinical trial of a proprietary investigational product and no plan currently exists for sharing individual participant data.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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