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Die klinische Studie NCT06959615 für Fortgeschrittener solider Tumor ist offene rekrutierung. In der Kartenansicht des Klinische Studien Radar und den KI-Entdeckungstools finden Sie alle Details. Oder stellen Sie hier Ihre Fragen.
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A Phase I/IIa Study of JAB-23E73 in Patients With Advanced Solid Tumors Harboring KRAS Gene Alteration Phase 1, Phase 2 334 Dosis-Eskalation Offene Studie

Offene Rekrutierung
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Die klinische Studie NCT06959615 untersucht Behandlung im Zusammenhang mit Fortgeschrittener solider Tumor. Diese interventionsstudie der Phase 1 Phase 2 hat den Status offene rekrutierung und startete am 22. November 2024. Es ist geplant, 334 Teilnehmer aufzunehmen. Durchgeführt von Jacobio Pharmaceuticals Co., Ltd. wird der Abschluss für 31. August 2027 erwartet. Die Daten von ClinicalTrials.gov wurden zuletzt am 20. Januar 2026 aktualisiert.
Kurzbeschreibung
This is a multicenter, open-label, phase I/IIa to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of pan-KRAS inhibitor JAB-23E73 in patients with advanced solid tumors harboring KRAS mutations or amplification. The study consists of 2 phases: Phase 1 Dose Escalation and Phase IIa Dose Expansion.
Ausführliche Beschreibung
Study JAB-23E73-1001 is a global multicenter, open-label Phase 1/2a study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anticancer activity of JAB-23E73 as a single agent in adult patients with advanced solid tumors with KRAS alteration. This study consists of a Phase 1a dose-escalation, followed by Phase 1b dose-expansion (dose optimization) and Phase 2a indication expansi...Mehr anzeigen
Offizieller Titel

A Multicenter, Open Phase I/IIa Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of JAB-23E73 in Patients With Advanced Solid Tumors Harboring KRAS Gene Alteration

Erkrankungen
Fortgeschrittener solider Tumor
Weitere Studien-IDs
  • JAB-23E73-1001
NCT-Nummer
Studienbeginn (tatsächlich)
2024-11-22
Zuletzt aktualisiert
2026-01-20
Studienende (vorauss.)
2027-08-31
Geplante Rekrutierung
334
Studientyp
Interventionsstudie
PHASE
Phase 1
Phase 2
Status
Offene Rekrutierung
Stichwörter
KRAS
KRAS mutation
KRAS G12C, KRAS G12D, KRAS G12V, KRAS G12S, KRAS G12A, KRAS G12D
Pan-KRAS
NSCLC
Pancreas cancer
Colorectal cancer
KRAS-mutant tumor
Targeted Therapy
JAB-23E73
Primäres Ziel
Behandlung
Zuteilungsmethode
Nicht randomisiert
Interventionsmodell
Sequentiell
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
ExperimentellPhase 1 Dose Exploration
Monotherapy, dose escalation
JAB-23E73
Administered orally
ExperimentellPhase 2a Dose Expansion
Monotherapy, dose expansion
JAB-23E73
Administered orally
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Phase 1: Number of participants with dose limiting toxicities (DLT)
Incidence of dose limiting toxicities (DLTs) in the dose escalation phase. DLTs will be defined as the occurrence of any of the toxicities as described in the protocol.
Up to 21 days
Phase 2a: Objective response rate (ORR)
ORR is defined as the proportion of patients with a best overall response (BOR) of confirmed complete response (CR) or confirmed partial response (PR) per RECIST v1.1.
Up to approximately 2 years
Nebenergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Phase 1/2a: Adverse events
Incidence and severity of treatment-emergent Adverse Events (TEAEs), treatment-related Adverse Events (TRAEs) and serious Adverse Events (SAEs)
Up to approximately 2 years
Phase 1/2a: Pharmacokinetic (PK): Maximum concentration (Cmax) of JAB-23E73
PK: Cmax of JAB-23E73
Up to approximately 2 years
Phase 1/2a: PK: Time to Maximum Concentration (Tmax) of JAB-23E73
PK: Tmax of JAB-23E73
Up to approximately 2 years
Phase 1/2a: PK: Area Under the Concentration Versus Time Curve (AUC) of JAB-23E73
PK: AUC of JAB-23E73
Up to approximately 2 years
Phase 1: ORR
ORR is defined as the proportion of patients with a BOR of confirmed CR or confirmed PR per RECIST v1.1.
Up to approximately 2 years
Phase 1/2a: Time to Response (TTR)
TTR is defined as the time from the date of first dose of study drug to first documentation of response as assessed by the investigator per RECIST v1.1
Up to approximately 2 years
Phase 1/2a: Progression Free Survival (PFS)
PFS is defined as the time from the date of the first dose of study drug to the date of the first documentation of progressive disease assessed by the investigator per RECIST v1.1 or death, whichever occurs first.
Up to approximately 2 years
Phase 1/2a: Disease Control Rate (DCR)
DCR is defined as the proportion of patients with CR, PR, or stable disease (SD) as assessed by the investigator per RECIST v1.1
Up to approximately 2 years
Phase 1/2a: Duration of Response (DoR)
DOR is defined as the time from the first determination of an objective response per RECIST v1.1 until the first documentation of disease progression or death, whichever occurs first as assessed by the investigator.
Up to approximately 2 years
Phase 2a: Overall Survival (OS)
OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
Up to approximately 2 years
Teilnahme-Assistent
Eignungskriterien

Zugelassene Altersgruppen
Kind, Erwachsene, Ältere Erwachsene
Zugelassene Geschlechter
Alle
  1. Histological or cytologically proven diagnosis of a locally advanced, unresectable, and/or metastatic solid tumor cancer with evidence of KRAS gene alteration (including gene mutation and wild type amplification).
  2. Able to provide an archived tumor tissue sample or fresh biopsy sample.
  3. Life expectancy ≥3 months at the start of treatment.
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  5. ≥1 measurable lesion per RECIST v1.1.
  6. Adequate organ function.

  1. Unable to swallow oral medications or with gastrointestinal dysfunction or gastrointestinal disease that significantly alters the absorption of medication.
  2. Previous treatment with rat sarcoma (RAS) targeting agents.
  3. Symptomatic, untreated, or actively progressing known central nervous system (CNS) metastases.
  4. Impaired cardiovascular function or clinically significant cardiac disease.
  5. Mean QT interval corrected using Fridericia's formula (QTcF) >470 msec.
  6. Females who are pregnant or breastfeeding.
Jacobio Pharmaceuticals Co., Ltd. logoJacobio Pharmaceuticals Co., Ltd.
Zentrale Studienkontakte
Kontakt: Jacobio Pharmaceuticals, 86 10 56315466, [email protected]
32 Studienstandorte in 1 Ländern

Anhui

Anhui Provincial Cancer Hospital, Hefei, Anhui, 230001, China
Noch nicht rekrutierend

Beijing Municipality

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, Beijing Municipality, 100021, China
Offene Rekrutierung
Beijing Cancer Hospital, Beijing, Beijing Municipality, 100032, China
Offene Rekrutierung
Beijing Chest Hospital, Beijing, Beijing Municipality, 100032, China
Offene Rekrutierung
Peking Union Medical College Hospital, Beijing, Beijing Municipality, 100032, China
Offene Rekrutierung
Beijing Friendship Hospital, Capital Medical University, Beijing, Beijing Municipality, 100050, China
Noch nicht rekrutierend

Fujian

Fujian cancer Hospital, Fuzhou, Fujian, 350014, China
Noch nicht rekrutierend

Guangdong

Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510120, China
Offene Rekrutierung

Guangxi

Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530012, China
Offene Rekrutierung

Hebei

National Cancer Center/Cancer Hospital- Langfang Campus, Chinese Academy of Medical Sciences and Peking Union Medical College, Langfang, Hebei, 065000, China
Offene Rekrutierung

Heilongjiang

Harbin Medical University Cancer Hospital, Haerbin, Heilongjiang, 150081, China
Offene Rekrutierung

Henan

Henan Cancer Hospital, Zhengzhou, Henan, 450003, China
Offene Rekrutierung
The First Affiliated hospital of Zhengzhou University, Zhengzhou, Henan, 450052, China
Offene Rekrutierung

Hubei

Tongji Hospital, Wuhan, Hubei, 430030, China
Noch nicht rekrutierend
Zhongnan Hospital of Wuhan University, Wuhan, Hubei, 430071, China
Offene Rekrutierung

Hunan

Hunan Cancer Hospital, Changsha, Hunan, 200032, China
Noch nicht rekrutierend

Jiangsu

Nanjing Drum Tower Hospital, Nanjing, Jiangsu, 210008, China
Offene Rekrutierung
Jiangsu Cancer Hospital, Nanjing, Jiangsu, 210009, China
Noch nicht rekrutierend
Jiangsu Province Hospital, Nanjing, Jiangsu, 210029, China
Offene Rekrutierung
The First Affiliate of Soochow University, Suzhou, Jiangsu, 215006, China
Noch nicht rekrutierend

Jiangxi

The First Affiliated hospital of Nanchang University, Nanchang, Jiangxi, 330006, China
Offene Rekrutierung

Liaoning

The First Hospital of China Medical University, Shenyang, Liaoning, 110001, China
Offene Rekrutierung

Shanghai Municipality

Shanghai Jiaotong University School of Medicine Ruijin Hospital, Shanghai, Shanghai Municipality, 200025, China
Noch nicht rekrutierend
Fudan University Zhongshan Hospital, Shanghai, Shanghai Municipality, 200032, China
Noch nicht rekrutierend
Huashan Hospital Fudan University, Shanghai, Shanghai Municipality, 200040, China
Noch nicht rekrutierend

Shanxi

ShanXi Cancer Hospital, Taiyuan, Shanxi, 650118, China
Offene Rekrutierung
The First Affiliated hospital of Xi'an Jiaotong University, Xi’an, Shanxi, 710061, China
Noch nicht rekrutierend

Sichuan

West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China
Noch nicht rekrutierend

Tianjin Municipality

Tianjin Medical University Cancer Institute&Hospital, Tianjin, Tianjin Municipality, 300211, China
Noch nicht rekrutierend

Zhejiang

Zhejiang Cancer Hospital, Hangzhou, Zhejiang, 310005, China
Offene Rekrutierung
The Second Affiliate Hospital Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310009, China
Noch nicht rekrutierend
Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, 310014, China
Noch nicht rekrutierend