- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07623356
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.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 2
- Fas 1
Kontakter och platser
Studiekontakt
- Namn: Xufang Yu
- Telefonnummer: +86 (0760) 89873999
- E-post: clinicaltrials@akesobio.com
Studieorter
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina
- Rekrytering
- Shanghai East Hospital
-
Kontakt:
- Caicun Zhou
- Telefonnummer: +8613301825532
- E-post: caicunzhoudr@163.com
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
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 non-small cell lung cancer (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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: AK138D1
AK138D1 will be administered at pre-specified dose levels.
|
Inskrivna försökspersoner kommer att få intravenös infusion (IV) av AK138D1 enligt den doseringsregim som anges i deras kohort.
|
|
Experimentell: AK138D1+ Ivonescimab
AK138D1 and ivonescimab will be administered at pre-specified dose levels.
|
Inskrivna försökspersoner kommer att få intravenös infusion (IV) av AK138D1 enligt den doseringsregim som anges i deras kohort.
Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.
|
|
Experimentell: AK138D1 + Ivonescimab + Carboplatin
AK138D1, ivonescimab and carboplatin will be administered at pre-specified dose levels.
|
Inskrivna försökspersoner kommer att få intravenös infusion (IV) av AK138D1 enligt den doseringsregim som anges i deras kohort.
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.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Adverse events (AEs)
Tidsram: Up to approximately 2 years
|
Incidence and severity of subjects with adverse events
|
Up to approximately 2 years
|
|
Objective Response Rate (ORR)
Tidsram: Up to approximately 2 years
|
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.
|
Up to approximately 2 years
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Anti-drog antikroppar (ADA)
Tidsram: Upp till cirka 2 år
|
Antal försökspersoner med detekterbara anti-läkemedelsantikroppar (ADA).
|
Upp till cirka 2 år
|
|
Total överlevnad (OS)
Tidsram: Upp till cirka 2 år
|
Total överlevnad (OS) definieras som tiden från randomisering till död på grund av någon orsak.
|
Upp till cirka 2 år
|
|
Disease Control Rate (DCR)
Tidsram: Up to approximately 2 years
|
Disease control rate (DCR) assessed by investigator according to RECIST v1.1.
|
Up to approximately 2 years
|
|
Duration of response (DoR)
Tidsram: Up to approximately 2 years
|
Duration of response (DoR) assessed by investigator according to RECIST v1.1.
|
Up to approximately 2 years
|
|
Time to response (TTR)
Tidsram: Up to approximately 2 years
|
Time to response (TTR) is defined as the time to response assessed by investigator according to RECIST v1.1.
|
Up to approximately 2 years
|
|
Pharmacokinetics (PK) characteristics
Tidsram: Up to approximately 2 years
|
Serum drug concentration profiles at different time points after administration.
|
Up to approximately 2 years
|
|
Progression Free Survival (PFS)
Tidsram: Up to approximately 2 years
|
Progression Free Survival (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.
|
Up to approximately 2 years
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- AK138D1-201
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .