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Dose Finding Safety Study of VAL201 in Cancer Patients (VAL201-001)

8 octobre 2021 mis à jour par: ValiRx Plc

A Phase I/II, Dose Escalation Study To Assess The Safety and Tolerability of VAL201 In Patients With Advanced or Metastatic Prostate Cancer and Other Advanced Solid Tumours

Dose finding safety study of VAL201 in cancer patients.

Aperçu de l'étude

Statut

Complété

Intervention / Traitement

Description détaillée

A Phase I/II, dose escalation study to assess the safety and tolerability of VAL201 in patients with locally advanced or metastatic prostate cancer and other advanced solid tumours.

Type d'étude

Interventionnel

Inscription (Réel)

12

Phase

  • Phase 2
  • La phase 1

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Homme

La description

The study will enrol patients with locally advanced or metastatic prostate cancer. The MTD/MAD may also be evaluated in patients with other advanced tumour types for whom no standard effective therapy is available and a rationale for use of VAL201 exists.

The average timeframe is 18-26 weeks per subject and the outcome measured is a composite average for each group.

  • Inclusion criteria:

    • Specific Inclusion Criteria for Patients with Prostate Cancer
    • Patients with incurable, locally advanced or metastatic prostate cancer where a policy of intermittent hormone therapy has been decided. Who have specific clinical parameters.
  • Specific Inclusion Criteria for Patients with Other Advanced Solid Tumours

    • Patients with histologically and/or cytologically confirmed advanced solid tumour for whom no standard effective therapy is available and a rationale for use of VAL201 exists.
    • Patients with incurable, locally advanced or metastatic prostate cancer where a policy of intermittent hormone therapy has been decided. These patients must also have the following:

      1. Rising PSA on three samples (once non-castrate levels established); each over 2 weeks apart, with the last two values being greater than 2 ng/mL. Higher than and at least 25% over the nadir.
      2. Absent or very mild prostate cancer-related symptoms.
      3. No plans for any therapy for prostate cancer in the next two months.
    • General Inclusion Criteria for all Patients
    • Adult patients defined by age greater than 18 years at time of consent.
    • Ability to give written, informed consent prior to any study-specific Screening procedures, with the understanding that the consent may be withdrawn by the patient at any time without prejudice.
    • Patient is capable of understanding the protocol requirements, is willing and able to comply with the study protocol procedures, and has signed the informed consent document.
    • Evaluable disease, either measurable on imaging, or with informative tumour marker(s) and a set of specific biochemical and haematological parameters relating to the specific cancer.
    • Negative human chorionic gonadotropin (hCG) test in women of childbearing potential.
    • Sexually active male and female patients of childbearing potential must agree to use an effective method of birth control. Female patients may be surgically sterile.
    • Laboratory values at Screening:

      • Absolute neutrophil count ≥1.5 x 109/L.
      • Platelets ≥100 x 109/L.
      • Haemoglobin ≥9 g/dL without blood transfusion or colony stimulating factor support.
      • Total bilirubin <1.5 times the upper limit of normal (ULN);
      • AST (SGOT) ≤2.5 times the ULN;
      • ALT (SGPT) ≤2.5 times the ULN; ≤5 x ULN for patients with advanced solid tumours with liver metastases.
      • Serum creatinine ≤1.5 x ULN or estimated glomerular filtration rate (GFR) of >50 mL/min based on the Cockcroft-Gault formula.
  • Exclusion criteria

    • Specific Exclusion Criteria for Patients with Prostate Cancer Patients has received an anticancer therapy, including investigational agents, within the precious 6 weeks or 4 weeks.
    • Any patients who have undergone prior orchidectomy.
    • Specific Exclusion Criteria for Patients with Other Advanced Solid Tumours Pregnant or lactating female patients.
    • Documented, symptomatic or uncontrolled brain metastases.
    • History of clinically significant cardiac condition, including ischemic cardiac event, myocardial infarction or unstable cardiac disease within 3 months previous to the indication of home therapy.
    • Known Human Immunodeficiency Virus positivity.
    • Active Hepatitis B or C or other active liver disease (other than malignancy).
    • Any active, clinically significant, viral, bacterial, or systemic fungal infection within previous 4 weeks prior to home therapy.
    • Any medical history that would jeopardize compliance.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Cohort 1: 0.5 mg/kg
VAL201-001 Sub-cutaneous injection. 0.5 mg/kg
VAL201-001 Sub-cutaneous injection.
Autres noms:
  • VAL201-001
Expérimental: Cohort 2: 1 mg/kg
VAL201-001 Sub-cutaneous injection. 1.0 mg/kg
VAL201-001 Sub-cutaneous injection.
Autres noms:
  • VAL201-001
Expérimental: Cohort 3: 2 mg/kg
VAL201-001 Sub-cutaneous injection. 2.0 mg/kg
VAL201-001 Sub-cutaneous injection.
Autres noms:
  • VAL201-001
Expérimental: Cohort 4: 4 mg/kg
VAL201-001 Sub-cutaneous injection. 4.0 mg/kg
VAL201-001 Sub-cutaneous injection.
Autres noms:
  • VAL201-001
Expérimental: Cohort 5: up to 8 mg/kg
VAL201-001 Sub-cutaneous injection. 8.0 mg/kg; potential to escalate to 16 mg/kg after 3 cycles according to clinician decision Flexibility of dosing enabled under protocol.
VAL201-001 Sub-cutaneous injection.
Autres noms:
  • VAL201-001

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Dose-Limiting Toxicity
Délai: The average timeframe is 18-26 weeks per subject
The number of Dose-Limiting Toxicity events is used to determine whether a maximum tolerated dose (MTD) is obtained.
The average timeframe is 18-26 weeks per subject

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pharmacokinetics of VAL201. (Cmax)
Délai: The average timeframe is 18-26 weeks per subject
Assessment of pharmacokinetic variables at multiple time points (5 min, 10 min, 15 min, 30 min, 60 min, 90 min, 2 hours, 3 hours, 4 hours, 6 hours and 8 hours after dosing) and multiple dosing days (Cycle 1 Day 1, Cycle 3 Day 1, Cycle 4 Day 1 and Cycle 6 Day 1) for each patient analysed.
The average timeframe is 18-26 weeks per subject
Pharmacokinetics of VAL201 (AUC 0-inf)
Délai: The average timeframe is 18-26 weeks per subject
Assessment of pharmacokinetic variables at multiple time points (5 min, 10 min, 15 min, 30 min, 60 min, 90 min, 2 hours, 3 hours, 4 hours, 6 hours and 8 hours after dosing) and multiple dosing days (Cycle 1 Day 1, Cycle 3 Day 1, Cycle 4 Day 1 and Cycle 6 Day 1) for each patient analysed.
The average timeframe is 18-26 weeks per subject

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Number of Patients Who Completed 6 Cycles of Treatment
Délai: The average timeframe is 18-26 weeks per subject
The number of patients who completed 6 cycles of treatment is compared with the number who withdrew prior to completion of the scheduled 6 cycles
The average timeframe is 18-26 weeks per subject
Number of Patients Displaying Disease Progression by PCWG2 and/or RECIST Criteria
Délai: The average timeframe is 18-26 weeks per subject
Assessment of disease response to treatment by PCWG2 and/or RECIST. Disease progression is defined by RECIST 1.1 as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions; and by PCWG2 criteria that PSA values did not see an increase of 25% or more and absolute increase of 2 ng/mL or more from the nadir.
The average timeframe is 18-26 weeks per subject

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 octobre 2014

Achèvement primaire (Réel)

27 janvier 2020

Achèvement de l'étude (Réel)

27 janvier 2020

Dates d'inscription aux études

Première soumission

20 octobre 2014

Première soumission répondant aux critères de contrôle qualité

28 octobre 2014

Première publication (Estimation)

31 octobre 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

8 novembre 2021

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 octobre 2021

Dernière vérification

1 octobre 2021

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • VAL201-001
  • 2013-004009-25 (Numéro EudraCT)

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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