- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT02280317
Dose Finding Safety Study of VAL201 in Cancer Patients (VAL201-001)
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
Tutkimuksen yleiskatsaus
Tila
Interventio / Hoito
Yksityiskohtainen kuvaus
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 2
- Vaihe 1
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
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:
- 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.
- Absent or very mild prostate cancer-related symptoms.
- 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informed consent prior to any study-specific Screening procedures, with the understanding that the consent may be withdrawn by the patient at any time without prejudice.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.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei satunnaistettu
- Inventiomalli: Peräkkäinen tehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Cohort 1: 0.5 mg/kg
VAL201-001 Sub-cutaneous injection.
0.5 mg/kg
|
VAL201-001 Sub-cutaneous injection.
Muut nimet:
|
|
Kokeellinen: Cohort 2: 1 mg/kg
VAL201-001 Sub-cutaneous injection.
1.0 mg/kg
|
VAL201-001 Sub-cutaneous injection.
Muut nimet:
|
|
Kokeellinen: Cohort 3: 2 mg/kg
VAL201-001 Sub-cutaneous injection.
2.0 mg/kg
|
VAL201-001 Sub-cutaneous injection.
Muut nimet:
|
|
Kokeellinen: Cohort 4: 4 mg/kg
VAL201-001 Sub-cutaneous injection.
4.0 mg/kg
|
VAL201-001 Sub-cutaneous injection.
Muut nimet:
|
|
Kokeellinen: 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.
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Dose-Limiting Toxicity
Aikaikkuna: 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
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Pharmacokinetics of VAL201. (Cmax)
Aikaikkuna: 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)
Aikaikkuna: 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
|
Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Number of Patients Who Completed 6 Cycles of Treatment
Aikaikkuna: 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
Aikaikkuna: 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
|
Yhteistyökumppanit ja tutkijat
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Arvio)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
- VAL201-001
- 2013-004009-25 (EudraCT-numero)
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