A Study of AK138D1 Alone or in Combination With Ivonescimab in Advanced Non-Small Cell Lung Cancer
A Phase Ib/II Study of AK138D1 as Monotherapy and in Combination With Ivonescimab in Patients With Advanced Non-Small Cell Lung Cancer
The goal of this clinical trial is to evaluate the safety, tolerability, and efficacy of AK138D1 as monotherapy or in combination with ivonescimab in patients with advanced non-small cell lung cancer.
Participants will receive study treatment with AK138D1 alone or in combination with ivonescimab, undergo safety assessments and tumor evaluations, and be followed for treatment tolerability, antitumor activity, and clinical outcomes.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Xufang Yu
- Telefonnummer: +86 (0760) 89873999
- E-mail: clinicaltrials@akesobio.com
Studiesteder
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Kina
- Shanghai East Hospital
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Kontakt:
- Caicun Zhou
- Telefonnummer: +8613301825532
- E-mail: caicunzhoudr@163.com
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- The subject must sign the written informed consent form (ICF) voluntarily;
- At enrollment, aged ≥ 18 to ≤ 75 years, both males and females are eligible;
- Has an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;
- Has a life expectancy of ≥ 3 months;
- Has measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
- Has Stage IIIB/IIIC or IV NSCLC (American Joint Committee on Cancer [AJCC]).
- Adequate organ function.
Exclusion Criteria:
- Concomitant participation in another clinical study, unless it is a non-interventional clinical study or the follow-up period of an interventional study;
- Presence of active central nervous system (CNS) metastases.
- Live vaccines or attenuated live vaccines administered within 4 weeks prior to the first dose, or planned to be administered during the study; use of inactivated vaccines is allowed;
- Untreated subjects with active hepatitis B or active hepatitis C;
- Known active pulmonary tuberculosis (TB); subjects with suspected active TB must undergo appropriate clinical assessment to rule out the presence of active disease;
- Known active syphilis infection;
- Subjects with known allergy to any component of any study drug; and with a history of known severe hypersensitivity reactions to other monoclonal antibodies;
- Other reasons for ineligibility as evaluated by investigator.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Eksperimentel: AK138D1
AK138D1 will be administered at pre-specified dose levels.
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Tilmeldte forsøgspersoner vil modtage intravenøs infusion (IV) af AK138D1 i henhold til det doseringsregime, der er specificeret i deres kohorte.
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Eksperimentel: AK138D1+ Ivonescimab
AK138D1 and ivonescimab will be administered at pre-specified dose levels.
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Tilmeldte forsøgspersoner vil modtage intravenøs infusion (IV) af AK138D1 i henhold til det doseringsregime, der er specificeret i deres kohorte.
Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.
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Eksperimentel: AK138D1 + Ivonescimab + Carboplatin
AK138D1, ivonescimab and carboplatin will be administered at pre-specified dose levels.
|
Tilmeldte forsøgspersoner vil modtage intravenøs infusion (IV) af AK138D1 i henhold til det doseringsregime, der er specificeret i deres kohorte.
Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.
Enrolled subjects will receive intravenous infusion (IV) of Carboplatin according to the dosing regimen specified in their cohort.
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Adverse events (AEs)
Tidsramme: Up to approximately 2 years
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Incidence and severity of subjects with adverse events
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Up to approximately 2 years
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Objective Response Rate (ORR)
Tidsramme: Up to approximately 2 years
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Objective Response Rate (ORR) is the proportion of subjects with complete response (CR) or partial response (PR) , assessed by investigator according to RECIST v1.1.
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Up to approximately 2 years
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Anti-lægemiddel-antistoffer (ADA)
Tidsramme: Op til cirka 2 år
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Antal forsøgspersoner med påviselige anti-lægemiddel-antistoffer (ADA).
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Op til cirka 2 år
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Samlet overlevelse (OS)
Tidsramme: Op til cirka 2 år
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Samlet overlevelse (OS) er defineret som tiden fra randomisering til død på grund af enhver årsag.
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Op til cirka 2 år
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Disease Control Rate (DCR)
Tidsramme: Up to approximately 2 years
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Disease control rate (DCR) assessed by investigator according to RECIST v1.1.
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Up to approximately 2 years
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Duration of response (DoR)
Tidsramme: Up to approximately 2 years
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Duration of response (DoR) assessed by investigator according to RECIST v1.1.
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Up to approximately 2 years
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Time to response (TTR)
Tidsramme: Up to approximately 2 years
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Time to response (TTR) is defined as the time to response assessed by investigator according to RECIST v1.1.
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Up to approximately 2 years
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Progression Free Survival (PFS)
Tidsramme: Up to approximately 2 years
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PFS is defined as the time from randomization to the first documented disease progression (per RECIST v1.1) assessed by investigator or death due to any cause, whichever occurs first.
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Up to approximately 2 years
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Pharmacokinetics (PK) characteristics
Tidsramme: Up to approximately 2 years
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Serum drug concentration profiles at different time points after administration.
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Up to approximately 2 years
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- AK138D1-201
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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