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- Klinische proef NCT07661797
Phase I Clinical Study of LNF2105 in Patients With Advanced Solid Tumors
16 juni 2026 bijgewerkt door: Shandong New Time Pharmaceutical Co., LTD
A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Antitumor Efficacy of LNF2105 in Patients With Advanced Solid Tumors.
This study is a Phase I clinical trial evaluating the safety, tolerability, pharmacokinetic characteristics, and preliminary antitumor efficacy of LNF2105 in patients with advanced solid tumors.
Studie Overzicht
Toestand
Nog niet aan het werven
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
294
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Shaohong Yin
- Telefoonnummer: 86-15265901803
- E-mail: yinshaohong@lunan.com.cn
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Male or female aged ≥18 years.
- Patients with advanced solid tumors (including but not limited to urothelial carcinoma, breast cancer, non-small cell lung cancer, ovarian cancer, endometrial cancer, and cervical cancer) that have been histologically or cytologically confirmed as having failed/cannot tolerate/have no standard treatment/are currently unsuitable for standard treatment.
- Able to provide previous Nectin-4 expression testing results or preserved/fresh tumor tissue for Nectin-4 expression testing.
- At least one measurable lesion (CT or MRI long axis ≥ 10 mm, lymph node short axis ≥ 15 mm) according to RECIST v1.1 criteria. For lesions previously treated with radiotherapy, they will only be included as measurable lesions if there has been clear disease progression after radiotherapy.
- The function of vital organs must meet the following requirements (no blood components or cytokines may be used within 14 days prior to the first dose).
7) ECOG score 0-1. 8) Expected survival ≥ 3 months. 9) Willing to participate and sign informed consent form, and willing to follow the trial treatment protocol and visitation plan.
Exclusion Criteria:
- Prior treatment with an antibody-drug conjugate (ADC) exhibiting one of the following characteristics: payload as a topoisomerase I inhibitor (TOP 1 inhibitor); antibody target as Nectin-4.
- Received any P-glycoprotein (P-gp) inducer/inhibitor, strong CYP3A inhibitor, or breast cancer resistance protein (BCRP) inhibitor within 14 days prior to first administration (see Appendix 3 for the exclusion list).
- Patients who received chemotherapy within 3 weeks or radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy, or other anti-tumor treatments within 4 weeks prior to first administration of the study drug, excluding the following.
- Patients who received systemic glucocorticoid therapy or any other form of immunosuppressive therapy (equivalent to a prednisone dose >10 mg/day) within 2 weeks prior to the first dose.
- Patients whose adverse reactions to previous antitumor therapy have not recovered to a CTCAE 5.0 grade ≤1 or the level specified in the inclusion/exclusion criteria (excluding toxicities deemed safe by the investigator, such as alopecia, grade 2 peripheral neurotoxicity, and stable hypothyroidism after hormone replacement therapy).
- Patients with primary central nervous system (CNS) malignancies, CNS metastases that have failed local treatment, or carcinomatous meningitis; patients with asymptomatic brain metastases, or stable clinical symptoms such as neurological symptoms and who do not require corticosteroids or other treatments targeting brain metastases for ≥4 weeks may be enrolled.
- Patients with uncontrollable pleural effusion, pericardial effusion, or ascites requiring repeated drainage.
- Patients with known interstitial lung disease (ILD) or non-infectious pneumonia, currently symptomatic or requiring prior systemic glucocorticoid therapy, whose toxicity assessment or management is deemed by the investigator to potentially affect the investigational treatment.
- Patients with a history of organ transplantation or allogeneic bone marrow transplantation, or who received autologous stem cell transplantation within 3 months prior to the first dose.
- Patients who underwent major surgery within 4 weeks prior to the first dose or have not yet recovered from surgery.
- Patients with any of the following laboratory findings.
- Patients with uncontrolled or severe cardiovascular disease, including those who developed NYHA Class II or higher congestive heart failure, unstable angina, myocardial infarction, or other cardiovascular diseases within 6 months prior to the first dose; or those with uncontrolled hypertension (systolic blood pressure ≥ 160 mmHg and/or diastolic blood pressure ≥ 100 mmHg after treatment).
- Patients with active infections requiring intravenous anti-infective therapy or a history of the following conditions, including but not limited to active autoimmune diseases, severe mental illness, severe endocrine disorders such as severe thyroid dysfunction.
- Patients with the following ocular diseases: a) active infection or corneal ulcer; b) history of corneal transplantation; c) expected contact lens wear during the study period; d) poorly controlled glaucoma; e) poorly controlled or progressive retinopathy, wet macular degeneration, uveitis, papilledema, or optic disc disease; f) or other currently existing ocular diseases that would affect the assessment of ocular toxicity after the trial intervention.
- Glycated hemoglobin (HbA1c) ≥ 8.0%.
- Suffering from severe and/or uncontrolled comorbidities, such as decompensated cirrhosis, nephrotic syndrome, uncontrolled metabolic disorders, active inflammatory bowel disease, gastrointestinal perforation, intestinal obstruction, or gastrointestinal bleeding.
- Having a bleeding tendency (e.g., abnormal coagulation function tests, clinically significant as determined by the investigator, or clinically significant bleeding symptoms as assessed by the investigator).
- Having received any other clinical trial drug/device treatment within 4 weeks prior to the first dose.
- Having a history of drug abuse or alcoholism within 6 months prior to the first dose.
- Having a history of severe allergies, or a known history of allergy to macromolecular protein preparations/monoclonal antibodies, or to any component of the investigational drug.
- Having received a live or attenuated live vaccine within 4 weeks prior to the first dose.
- Pregnant or breastfeeding women, female participants of childbearing age, or male participants whose partners are women of childbearing age who do not agree to use medically approved effective contraception (such as an intrauterine device or condom) during the study period and for 6 months after the last study drug treatment.
- Individuals deemed unsuitable for enrollment by the investigator.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: LNF2105
The dosage was increased sequentially from 0.3 mg/kg, 0.6 mg/kg, 1.2 mg/kg, 2.0 mg/kg, 3.0 mg/kg, to 4.5 mg/kg.
|
The dosage of LNF2105 was increased sequentially from 0.3 mg/kg, 0.6 mg/kg, 1.2 mg/kg, 2.0 mg/kg, 3.0 mg/kg, to 4.5 mg/kg.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
To evaluate of Safety and Tolerability of LNF2105 in Patients with Advanced Solid Tumors
Tijdsspanne: Approximately 24months
|
Numbers of treatment emergent adverse events with severity determined using NCI CTCAE v6.0 after single or multiple doses of LNF2105.
|
Approximately 24months
|
|
To confirm Dose Limiting Toxicities (DLT) and determine MTD and RP2D for LNF2105
Tijdsspanne: 28 days
|
Occurrence of Dose Limiting Toxicities as defined in the protocol
|
28 days
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Maximum observed plasma concentration of LNF2105 (ADC), Total Antibody and Free Payload (Cmax)
Tijdsspanne: Approximately 24 months
|
Maximum observed plasma concentration ofLNF2105 (ADC), Total Antibody and Free Payload after single and multiple doses
|
Approximately 24 months
|
|
Time to reach Cmax of LNF2105 (ADC), Total Antibody and Free Payload (Tmax)
Tijdsspanne: 24 month
|
The amount of time to reach Cmax after single and multiple dose administration of LNF2105 (ADC), Total Antibody and Free Payload
|
24 month
|
|
Total Area Under the plasma concentration-time curve of LNF2105 (ADC), Total Antibody and Free Payload (AUC)
Tijdsspanne: 24 month
|
Area under the plasma concentration versus time curve after single and multiple dose administration of LNF2105 (ADC), Total Antibody and Free Payload
|
24 month
|
|
Minimum Plasma Concentration (Cmin) of LNF2105 (ADC), Total Antibody and Free Payload
Tijdsspanne: 24 month
|
Minimum Plasma Concentration (Cmin) of of LNF2105 (ADC), Total Antibody and Free Payload after multiple doses
|
24 month
|
|
To evaluate the preliminary antitumor activity of LNF2105: Overall response rate (ORR)
Tijdsspanne: Approximately 24months
|
ORR per investigator assessed Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1)
|
Approximately 24months
|
|
To evaluate the preliminary antitumor activity of LNF2105: Progression free survival (PFS)
Tijdsspanne: Approximately 24months
|
PFS per investigator assessed RECIST 1.1
|
Approximately 24months
|
|
To evaluate the preliminary antitumor activity of LNF2105: Duration of response (DOR)
Tijdsspanne: Approximately 24months
|
Anti-tumor preliminary efficacy will be evaluated of LNF2105 in accordance with RECIST v1.1
|
Approximately 24months
|
|
To evaluate the preliminary antitumor activity of LNF2105: Disease control rate (DCR)
Tijdsspanne: Approximately 24months
|
DCR per investigator assessed RECIST 1.1
|
Approximately 24months
|
|
To evaluate the preliminary antitumor activity of LNF2105: Time to response (TTR)
Tijdsspanne: Approximately 24months
|
TTR per investigator assessed RECIST 1.1
|
Approximately 24months
|
|
To evaluate the preliminary antitumor activity of LNF2105: Overall survival (OS)
Tijdsspanne: Approximately 24months
|
OS per investigator assessed RECIST 1.1
|
Approximately 24months
|
|
To evaluate the immunogenicity of LNF2105
Tijdsspanne: Approximately 24months
|
To evaluate the levels of anti-drug antibody (ADA) generated by study participants.
Confirmatory testing will be performed on ADA-positive samples; confirmed positive samples will undergo subsequent titer determination as appropriate.
|
Approximately 24months
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
1 juni 2026
Primaire voltooiing (Geschat)
1 juni 2028
Studie voltooiing (Geschat)
1 augustus 2028
Studieregistratiedata
Eerst ingediend
8 april 2026
Eerst ingediend dat voldeed aan de QC-criteria
16 juni 2026
Eerst geplaatst (Werkelijk)
22 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
22 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
16 juni 2026
Laatst geverifieerd
1 april 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- NTP-LNF2105-001
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
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