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A Phase I Study of JLM019 Injection (JLM019)

28 maggio 2026 aggiornato da: Jecho Biopharmaceuticals Co., Ltd.

A Phase I Study to Evaluate the Safety and Tolerability of JLM019 Injection in Patients With Advanced Malignancies

This is a multicenter, single-arm, open-label, dose escalation phase (Part A) and dose expansion (Part B) study to evaluate the safety and tolerability of JLM019 Injection in patients with advanced malignancies.

The study subjects are adults with advanced malignancies including advanced solid tumors or relapsed/refractory lymphoma.

During the dose escalation phase, the dose escalation scheme is the accelerated titration in 0.001 - 0.2 mg/kg cohorts plus a traditional '3 + 3' design in 0.6 - 10 mg/kg cohorts, jointly in nine dose cohorts 0.001, 0.01, 0.05, 0.2, 0.6, 1.5, 3, 6 and 10 mg/kg. JLM019 Injection is intended to be administered once a week (QW). However, the dose and interval of administration may be adjusted based on the acquired PK, PD, and safety data. Each treatment cycle is 28 days.The repeated dose is tentatively scheduled to be administered once weekly until one of the following occurs: disease progression, intolerable toxicity, requirement for new antitumor therapy, withdrawal of informed consent form, death, loss to follow-up, or other protocol-specified discontinuation conditions.

Safety profile, DLT, MTD and RED of JLM019 Injection shall be assessed during and after treatment, with PK, PD, immunogenicity and Efficacy analyzed correspondingly.

Panoramica dello studio

Descrizione dettagliata

1. Dose Escalation Rules

  1. If one Grade ≥ 2 treatment-emergent adverse event (TEAE) during the DLT observation period after the first dose at any dose level in Part A Dose Escalation will Add one more enrolled participant. If the supplementary enrolled subject also experiences ≥Grade 2 treatment-emergent adverse event will trigger the transition from accelerated titration to the traditional '3 + 3' cohort design.
  2. At the '3 + 3' dose escalation stage, a sentinel cohort will be employed. If no DLTs occur in the sentinel cohort within 14 days after the drug administration, the other two patients will be enrolled at once in this dose group. If DLTs occur in the sentinel cohort, the other two patients will also be enrolled sequentially.
  3. At the '3 + 3' dose escalation stage,

    1. If the first 3 patients at this dose level experience no DLTs during the observation period, the dose will be escalated.
    2. If 1 of the first 3 patients experienced DLTs or 2 of the first 3 patients of a cohort have Grade ≥ 2 CRS or neurotoxicity, another 3 patients will be enrolled in this group again, and dose escalation will be evaluated based on these 6 patients:
    3. If 1 of 6 patients experience DLTs, the dose will be escalated.
    4. If ≥ 2 of 6 patients experience DLTs, the dose escalation will be stopped.
    5. If ≥ 2 of the first 3 patients experienced DLTs, the dose escalation will be stopped.
  4. If MTD is reached at the starting dose level, a lower dose level will be considered.
  5. Upon completion of DLT observation for each dose level, SRC will determine whether to terminate dose escalation or continue for further escalation or expand the dose groups based on a comprehensive review of the collected data.
  6. The Recommended Expansion Dose (RED) will be determined based on the assessments of safety, efficacy, and PK data, regardless of whether the MTD is achieved.

2. Statistical Analysis 2.1 Safety Analysis AEs will be coded using the Medical Dictionary for Regulatory Activities (MedDRA). AEs will be graded according to NCI CTCAE v6.0. AEs will be summarized by treatment group, System Organ Class (SOC), and Preferred Term (PT). Summaries will include (but not limited to): number of cases and incidence rates for all AEs, drug-related AEs, serious AEs (SAEs), drug-related SAEs, AEs leading to treatment discontinuation, and fatal AEs. For clinical safety assessments (laboratory tests, vital signs, physical examinations, 12-lead ECGs, etc.), treatment related changes from baseline will be described. Treatment-emergent abnormal findings will be listed in tables. During the dose-escalation phase, the incidence of DLTs will be calculated for each dose cohort.

2.2 PK Analysis Drug concentration data in peripheral blood will be analyzed by dose cohort according to scheduled PK sampling time-points. Individual and mean concentration-time profiles will be plotted for each dose cohort using both linear and semi-logarithmic scales. For summary statistics (e.g., mean concentration) and mean profile plots: Scheduled PK sampling time will be used. For individual patient concentration-time curves: Actual PK sampling time will be used.

PK parameters including: Cmax, Tmax, t1/2, AUC0~inf, AUC0~t, CL/F, and Vz/F, will be analyzed by using non-compartmental analysis (NCA) for each dose cohort. Descriptive statistics will include number of subjects (n), arithmetic mean, standard deviation (SD), coefficient of variation (CV%), minimum, and maximum. For key parameters (e.g., Cmax and AUC0-inf), geometric mean and geometric CV% will also be reported.

2.3 PD Analysis Descriptive statistical methods will be used to analyze PD parameters by treatment groups. Time-course profiles of PD markers will be plotted.

2.4 ADA Analysis Descriptive summaries will be provided for the time and the proportion of ADA-positive subjects following investigational drug administration. ADA positive subjects will undergo Nab testing, and the time and incidence of Nab occurrence will be summarized.

2.5 Efficacy Analysis ORR and DCR will be reported as the number and percentage of subjects in each dose cohort, with 95 % confidence intervals (CIs) estimated by using the Clopper-Pearson method. For time-to-event endpoints (PFS, DOR, OS), median survival duration and corresponding 95 % CIs will be estimated for each dose cohort by using the Kaplan-Meier method. Kaplan-Meier survival curves will be plotted for the event occurrence over the time.

Tipo di studio

Interventistico

Iscrizione (Stimato)

115

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

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100730
        • Reclutamento
        • Peking Union Medical College Hospital
        • Contatto:
          • Ba yi, Doctor of Medicine
          • Numero di telefono: 86+010-69158373
          • Email: bayi@tjmuch.com
        • Contatto:
          • Han xiaohong, Doctor of Medicine
          • Numero di telefono: 86+010- 69154796

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:

  1. Eighteen years of age or older;
  2. Patients with histopathologically or cytologically confirmed advanced solid tumors (AST) or relapsed/refractory (r/r) Hodgkin's/Non-Hodgkin's lymphomas (HL/NHL, including transformed lymphomas):

    • AST subtypes include but are not limited: colorectal cancer (CRC), head and neck squamous cell carcinoma (HNSCC), hepatocellular carcinoma (HCC), non-small cell lung cancer (NSCLC), gastric cancer (GC), ovarian cancer (OV), renal cell carcinoma (RCC), melanoma, biliary tract cancer (BTC), alveolar soft part sarcoma (ASPS), etc.
    • HL/NHL subtypes include but are not limited: classical Hodgkin lymphoma (cHL), diffuse large B-cell lymphoma (DLBCL), high-grade B-cell lymphoma (HGBL), mantle cell lymphoma (MCL), etc.
  3. Measurable disease as defined as:

    • AST: At least one tumor lesion ≥ 10 mm in the longest diameter as assessed by computed tomography (CT);
    • HL/NHL: Fluorodeoxyglucose (FDG) avid disease by positron emission tomography (PET) and ≥ 1 lesion > 15 mm in the longest diameter by > 10 mm in the short axis, as assessed by CT;
  4. Patients with the following molecular profiles will be prioritized for enrollment:

    • High tumor T-cell infiltration (e.g., elevated T-cell GEP score);
    • TMB > 10 mut/Mb、MSI-H/dMMR status or POLE/POLD1 mutations. Absence of β2M and JAK1/JAK2 loss-of-function mutations.
  5. Submission of tumor biopsy representative of the current disease, which may consist of any of the following:

    • Archived formalin-fixed paraffin-embedded (FFPE) tissue block;
    • At least 15-20 slides of tumor tissue from an FFPE block suitable for immunohistochemistry (IHC), including ≥ 10 % tumor content per section with ≥ 20 mm2 of evaluable tissue which may include ≤ 50 % tumor adjacent tissue;
    • A fresh tumor biopsy obtained by surgical excision or core needle procedure prior to the first dose of JLM019 Injection;
  6. For patients with accessible tumors, willingness to undergo on-study biopsy as scheduled in the protocol;
  7. Eastern Cooperative Oncology Group (ECOG) performance status grade 0~1;
  8. Life expectancy ≥ 3 months estimated by the Investigator;
  9. Recovery to Grade ≤ 1 for any non-laboratory toxicity resulting from previous anticancer therapy prior to the first dose of investigational product (except alopecia, hearing loss, Grade ≤ 2 neuropathy, or endocrinopathy managed with replacement therapy);
  10. Adequate baseline hematologic, renal, hepatic, and cardiac function as defined by:

    • Lymphocyte ≥ 0.5 × 109/L;
    • ANC ≥ 1.5 × 109/L;
    • Platelet count (PLT) ≥ 100 × 109/L;
    • Hemoglobin (HGB)≥ 90 g/L (no packed red blood cell transfusion within the prior 2 weeks);
    • Serum total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN) or ≤ 3 × ULN for patients with Gilbert's disease;
    • Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m2, as calculated by the Modification of Diet in Renal Disease (MDRD) formula;
    • ALT and AST ≤ 2.5 × ULN (≤ 5 × ULN if there is evidence of hepatic involvement by malignant disease);
    • International normalized ratio (INR) or prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤1.5 × ULN unless the patient is receiving anticoagulant therapy in which PT or aPTT is within therapeutic range of intended use of anticoagulants;
    • High sensitivity cardiac troponin I (hs-cTnI) and N-terminal pro B-type natriuretic peptide (NT-proBNP) ≤ ULN (asymptomatic abnormalities may be permitted after clearance by cardiology consultation).
  11. All patients and their partners must have no plans for conception from screening period and during the trial, and agree to practice effective contraception during the trial and for 4 months after the last dose of JLM019.
  12. Able to participate and willing to give written informed consent form.

Exclusion Criteria:

  1. Allergy to JLM019 Injection components;
  2. History of Grade 4 infusion-related, anaphylactic or allergic reaction to any previous monoclonal antibody or other Fc-based protein therapy;
  3. Experienced any cardiovascular immune-related adverse event (irAE), or discontinued from that treatment due to a Grade 3 or higher irAE in previous ICI therapy;
  4. Any serious or uncontrolled health conditions listed below:

    • Patients with concurrent infections requiring intravenous antimicrobial therapy within the past 2 weeks, or with unexplained fever (body temperature ≥ 37.5 °C);
    • History of vascular diseases within the past 6 months (including myocardial infarction, unstable angina, cerebrovascular diseases, and peripheral arterial or aortic diseases);
    • Uncontrolled hypertension (defined as systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg on at least two separate occasions after antihypertensive treatment);
    • Individuals with active thrombosis, active bleeding, or pathological conditions associated with high bleeding risk (such as coagulation disorders);
    • Has an active autoimmune disease that has required systemic treatment (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment;
    • Any serious or uncontrolled cardiovascular condition, including but not necessarily limited to:

      1. Any history of myocarditis of any etiology;
      2. History of New York Heart Association Class III or IV congestive heart failure, myocardial infarction, unstable angina, cerebrovascular accident, cardiac hospitalization, or other acute uncontrolled heart disease within 6 months of scheduled C1D1;
      3. Left ventricular ejection fraction < 45 % on screening echocardiogram;
      4. Any clinically significant findings on screening EKG such as atrial or ventricular arrythmia (other than sinus tachycardia) or AV conduction abnormality such as left bundle branch block (such patients may be enrolled after cardiology clearance and Sponsor approval);
  5. History of (non-infectious) pneumonitis / interstitial lung disease or current pneumonitis / interstitial lung disease;
  6. Presence of any active central nervous system (CNS; brain or leptomeningeal) metastases. Solid tumor patients with CNS metastases are eligible if previously treated and there is no magnetic resonance imaging (MRI) evidence of progression for ≥ 8 weeks after treatment is complete and within 28 days prior to first dose of JLM019 Injection;
  7. Prior organ allograft or allogeneic hematopoietic stem cell transplantation (HSCT). Lymphoma patients ≥ 3 months post-HSCT with no evidence of active graft versus host disease may be eligible upon approval by the Investigator or Sponsor;
  8. Receipt of any of the following within the timeframes indicated, before first scheduled dose of JLM019 Injection:

    1. Checkpoint inhibitors, including PD-(L)1 (e.g., pembrolizumab, nivolumab, cemiplimab, avelumab, durvalumab), CTLA-4 (e.g., ipilimumab, tremelimumab) and Lag-3 (e.g., relatlimab), or costimulatory agonists (including but not limited to CD28, CD134 (OX40), CD137 (4-1BB)): 3 months (135 days for atezolizumab);
    2. Chemotherapy, small molecule anticancer agents (e.g., kinase inhibitors), or radiation: 2 weeks. Note: for lung cancers or mesotheliomas, radiation therapy to the lung that is > 30 Gy within 6 months;
    3. Other monoclonal antibodies, antibody-drug conjugates, bispecific antibodies, antibody-like drugs, cytokines, cell therapies, or radio immunoconjugates: 4 weeks (2 weeks permissible with documented disease progression and approval by the medical monitor or Sponsor);
  9. Currently participating in another clinical trial or has participated in another clinical trial within 4 weeks prior to the first dose of the investigational study treatment. Note: Patients who have entered the follow-up phase of another study may be enrolled if at least 4 weeks have elapsed since their last dose of study treatment;
  10. Any condition requiring systemic treatment with either corticosteroids (> 10 mg/day prednisone or equivalent) or other immunosuppressive medications within 14 days of the first dose of JLM019 Injection. Inhaled, intranasal or topical corticosteroids or adrenal replacement doses of corticosteroids are permitted in the absence of active autoimmune disease;
  11. Received a live or live-attenuated vaccine within 30 days prior to the first dose of JLM019 Injection. Note: Administration of inactivated vaccines is allowed;
  12. Received radiotherapy within 2 weeks of start of study treatment or had a history of radiation pneumonitis. Note: Patients must have recovered from all radiation-related toxicities, not required corticosteroids, and show no evidence of radiation pneumonitis. A 1-week washout period is permitted for palliative radiation (≤ 2 weeks of radiotherapy) to non-CNS disease;
  13. Any second malignancy active within the previous 3 years( (except adequately treated carcinoma in situ of cervix, basal cell carcinoma or squamous cell skin carcinoma));
  14. Patients with a history of AIDS, syphilis, or active hepatitis [For hepatitis B: positive hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and HBV-DNA copy number above the upper limit of quantification; for hepatitis C: positive HCV antibody and HCV RNA copy number above the upper limit of quantification].
  15. Pregnancy or lactation, and a woman of childbearing potential (WOCBP) who has a positive pregnancy test (within 7 days) prior to treatment;
  16. Patients deemed unsuitable for participation in this study at the Investigator's discretion.

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: JLM019 Injection

The JLM019 Injection will be administered via intravenous (IV) infusion at dose levels of 0.001, 0.01, 0.05, 0.2, 0.6, 1.5, 3, 6, and 10 mg/kg.

Each IV infusion must last at least 30 min. The repeated dose is tentatively scheduled to be administered once weekly until one of the following occurs: disease progression, intolerable toxicity, requirement for new antitumor therapy, withdrawal of informed consent form, death, loss to follow-up, or other protocol-specified discontinuation conditions. (Note: The dose and administration interval may be adjusted based on acquired PK, PD and safety data).

The JLM019 Injection will be administered via intravenous (IV) infusion at dose levels of 0.001, 0.01, 0.05, 0.2, 0.6, 1.5, 3, 6, and 10 mg/kg. Each IV infusion must last at least 30 min. The repeated dose is tentatively scheduled to be administered once weekly until one of the following occurs: disease progression, intolerable toxicity, requirement for new antitumor therapy, withdrawal of informed consent form, death, loss to follow-up, or other protocol-specified discontinuation conditions. (Note: The dose and administration interval may be adjusted based on acquired PK, PD and safety data).

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of participants with reported Dose-limiting toxicity (DLT)
Lasso di tempo: Within 28 days after the first dose
Evaluate according to the DLT standards specified in the protocol
Within 28 days after the first dose
Rate of adverse events
Lasso di tempo: Up to 3 years
In accordance with NCI CTCAE v5.0, the toxicity assessment will be conducted
Up to 3 years
Determine the recommended dose for combination for JLM019 injection
Lasso di tempo: Up to 3 years
Evaluate the data from the Phase Ia study to determine recommended dose for combination for JLM019 injection in Phase Ib
Up to 3 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Determination of JLM019 concentrations
Lasso di tempo: Up to 12 months
Assays were performed by ELISA at the central laboratory
Up to 12 months
Detection of anti-JLM019 antibodies in serum
Lasso di tempo: Up to 12 months
Assays were performed by ELISA at the central laboratory
Up to 12 months
Determination of detailed blood lymphocyte subsets
Lasso di tempo: Up to 12 months
Assays were performed by flow cytometry at the central laboratory
Up to 12 months
Determination of cytokines in blood
Lasso di tempo: Up to 12 months
Assays were performed by ELISA at the central laboratory
Up to 12 months
Objective response rate
Lasso di tempo: Up to 12 months
Assessed according to RECIST 1.1 based on radiological examinations (CT/MRI/ultrasound)
Up to 12 months
Disease control rate
Lasso di tempo: Up to 12 months
Assessed according to RECIST 1.1 based on radiological examinations (CT/MRI/ultrasound)
Up to 12 months
Progression-free survival
Lasso di tempo: Up to 15 years
Evaluated via regular follow-up; Disease progression is determined per RECIST 1.1
Up to 15 years
Duration of response
Lasso di tempo: Up to 15 years
Evaluated via regular follow-up ; Disease progression is determined per RECIST 1.1
Up to 15 years
Overall survival
Lasso di tempo: Up to 15 years
Evaluated via regular follow-up ; Disease progression is determined per RECIST 1.1
Up to 15 years

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 (Effettivo)

13 gennaio 2026

Completamento primario (Stimato)

14 marzo 2029

Completamento dello studio (Stimato)

1 luglio 2029

Date di iscrizione allo studio

Primo inviato

18 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 maggio 2026

Primo Inserito (Effettivo)

3 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

3 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 maggio 2026

Ultimo verificato

1 maggio 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)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

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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