- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07636707
QLF4113 in Participants With Metastatic Prostate Cancer
An Open-label, Multicenter Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of QLF4113 for Injection in Participants With Metastatic Prostate Cancer.
This is an open-label, dose-escalation and expansion Phase I clinical trial designed to evaluate the safety, tolerability, pharmacokinetic (PK) profile, immunogenicity, and preliminary antitumor activity of QLF4113 monotherapy in participants with metastatic prostate cancer.
The Phase I trial consists of two parts: Phase Ia and Phase Ib. Phase Ia is a dose-escalation study of QLF4113 monotherapy to determine the recommended phase two dose and assess safety and PK. Then the study will proceed to Phase Ib, a dose-expansion study to further evaluate the preliminary efficacy and safety of QLF4113 monotherapy under the selected doses.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Jun Guo, Doctor
- Numéro de téléphone: 0086-10- 88121122
- E-mail: guoj307@126.com
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Participants voluntarily agree to participate and sign the informed consent form.
- Male, aged ≥18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1.
- Life expectancy ≥ 3 months.
- Histologically or cytologically confirmed adenocarcinoma of the prostate without evidence of neuroendocrine carcinoma or small cell carcinoma features.
- Confirmed metastatic Castration-Resistant Prostate Cancer (mCRPC).
- Failed or are intolerant to standard therapies
- Adequate function of major organs as defined by the protocol.
- Agreement to use effective contraception during the study (except for subjects who have undergone bilateral orchiectomy).
- Prior to the first use of the investigational drug, recovery from all reversible adverse events (AEs) related to prior anticancer treatments
Exclusion Criteria:
- Previously treated with drugs targeting CD3 or CD2.
- Significant Cardiovascular Diseases
- Active, Uncontrolled Infections
- Immunosuppressive Treatment before the first dose of the investigational drug
- Clinically Uncontrolled Third-Space Fluid Accumulation
- History of Other Malignancies within 5 years prior to the first dose of the investigational drug
- Moderate to Severe Pulmonary Diseases significantly affecting lung function,
- Current Hepatic Encephalopathy, Hepatorenal Syndrome, or Cirrhosis classified as Child-Pugh B or worse.
- Allergy to the Investigational Drug or its Components.
- Any Condition deemed by the investigator to increase study-related risks, interfere with the interpretation of study results, or otherwise render the participant unsuitable for inclusion.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: QLF4113 dose escalation arm
|
A PSMA/CD3/CD2 antibody
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Maximum tolerated dose (MTD) (Phase Ia)
Délai: From first dose of study treatment until the end of Cycle 1 (21 days)
|
Maximum tolerated dose is defined as the previous dose level at which 2 or more out of 2-6 participants experienced a dose-limited toxicity (DLT).
|
From first dose of study treatment until the end of Cycle 1 (21 days)
|
|
Maximum administered dose (MAD)(Phase Ia)
Délai: From first dose of study treatment until the end of Cycle 1 (21 days)
|
MAD is defined as follows: a) based on PK data, it is anticipated that at this dose level, the dose-exposure plateau has been reached, b) based on existing safety data, it is judged that dose escalation following this dose level will have a large safety risk or subject intolerance, or c) based on the PK-PD model, it suggested that the optimal target concentration of safety and efficacy has been explored.
|
From first dose of study treatment until the end of Cycle 1 (21 days)
|
|
recommended phase II dose (RP2D)
Délai: Through phase Ia completion, approximately 1 year.
|
The RP2D will be comprehensively evaluated based on the safety, PK characteristics, and efficacy data from the Phase Ia study.
|
Through phase Ia completion, approximately 1 year.
|
|
The incidence and severity of adverse events (AE) (Phase Ib)
Délai: Through phase Ia completion, approximately 1 year.
|
Incidence and severity of adverse events (AEs) evaluated according to the National Cancer Institute (NCI)-Common Terminology Criteria for Adverse Events (CTCA) Version 6.0 (v6.0) and American Society for Transplantation and Cellular Therapy (ASTCT)
|
Through phase Ia completion, approximately 1 year.
|
|
PSA50 response (Phase Ib)
Délai: From Screening to confirmed progressive disease (approximately 1 year)
|
Best response until progression, as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version (v1.1) and Prostate Cancer Clinical Trials Working Group 3 (PCGW3).
|
From Screening to confirmed progressive disease (approximately 1 year)
|
|
Objective response rate (ORR) (phase Ib)
Délai: From Screening to confirmed progressive disease (approximately 1 year)
|
From Screening to confirmed progressive disease (approximately 1 year)
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies urogénitales
- Maladies génitales
- Tumeurs génitales, homme
- Tumeurs urogénitales
- Tumeurs par site
- Tumeurs
- Maladies génitales, sexe masculin
- Maladies de la prostate
- Maladies urogénitales masculines
- Tumeurs prostatiques
- Thérapeutique
- Voies d'administration du médicament
- Pharmacothérapie
- Injections
Autres numéros d'identification d'étude
- QLF4113-101
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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