A Dose Escalation, Dose Expansion Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-575, in Subjects With Advanced Tumors. (MEDI-575)
3 kwietnia 2018 zaktualizowane przez: MedImmune LLC
A Phase 1, Multicenter, Open-label, Single-arm, Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-575, a Fully Human Monoclonal Antibody Directed Against Platelet-derived Growth Factor Receptor Alpha (PDGFRα), in Subjects With Advanced Solid Tumors Refractory to Standard Therapy or for Which No Standard Therapy Exists
Evaluate the safety, tolerability and the tolerated maximum dose of MEDI-575 in adult subjects with advanced solid tumors refractory to standard therapy or for which no standard therapy exists.
Przegląd badań
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
49
Faza
- Faza 1
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
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Colorado
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Denver, Colorado, Stany Zjednoczone
- Research Site
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Indiana
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Indianapolis, Indiana, Stany Zjednoczone
- Research Site
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Nevada
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Las Vegas, Nevada, Stany Zjednoczone
- Research Site
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Texas
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Dallas, Texas, Stany Zjednoczone
- Research Site
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Virginia
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Norfolk, Virginia, Stany Zjednoczone
- Research Site
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
18 lat i starsze (Dorosły, Starszy dorosły)
Akceptuje zdrowych ochotników
Nie
Płeć kwalifikująca się do nauki
Wszystko
Opis
Inclusion Criteria:
- Histologically confirmed advanced solid tumor for which no curative or standard therapies exist
- Karnofsky performance status of ≥ 60
- Life expectancy of >12 weeks
- Adequate hematologic and organ function
- Negative serum pregnancy test (women only)
- Two methods of birth control for female participants of child-bearing potential or male participants with their female partners of child-bearing potential
Exclusion Criteria:
- Prior chemotherapy or investigational treatment within 4 weeks of study drug administration
- Prior biological or immunological treatment within 6 weeks of study drug administration
- Concurrent therapy for of cancer
- Major surgery within four weeks or minor surgery within two weeks of study drug administration
- History of diabetes or current treatment for diabetes
- New York Heart Association ≥ Grade 2 congestive heart failure
- History of myocardial infarction, unstable angina, transient ischemic attack or stroke within the previous 6 months prior to study entry
- History of other invasive malignancy within 5 years (exceptions are cervical carcinoma in situ, non-melanomatous carcinoma of the skin or ductal carcinoma in situ of the breast that are surgically cured)
- Significant active infection
- Known brain metastases
- Pregnancy or lactation or plans to become pregnant while on study
- Clinically significant abnormality on ECG
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: MEDI-575, 3.0 mg/kg QWk Escalation Phase (Cohort 1)
Single lead-in dose of MEDI-575 at 0.5 mg/kg as a 60-minute intravenous (IV) infusion administered 7 days prior to first dose at 3.0 mg/kg; MEDI-575 administered at 3.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (once every 7 days [QWk]) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 6.0 mg/kg QWk Escalation Phase (Cohort 2)
MEDI-575 administered at 6.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (QWk) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 9.0 mg/kg QWk Escalation Phase (Cohort 3)
MEDI-575 administered at 9.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (QWk) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 12 mg/kg QWk Escalation Phase (Cohort 4)
MEDI-575 administered at 12.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (QWk) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 15 mg/kg QWk Escalation Phase (Cohort 5)
MEDI-575 administered at 15.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (QWk) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 25 mg/kg Q3Wk Escalation Phase (Cohort 6)
MEDI-575 administered at 25.0 mg/kg as a 90-minute IV infusion on Study Day 1 of each 21-day treatment cycle (once every 21 days [Q3Wk]) until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 35 mg/kg Q3Wk Escalation Phase (Cohort 7)
MEDI-575 administered at 35.0 mg/kg as a 90-minute IV infusion on Study Day 1 of each 21-day treatment cycle (Q3Wk) until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 9.0 mg/kg QWk Expansion Phase
MEDI-575 administered at 9.0 mg/kg as a 60-minute IV infusion on Study Days 1, 8, and 15 (QWk) of each 21-day treatment cycle until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Eksperymentalny: MEDI-575, 25 mg/kg Q3Wk Expansion Phase
MEDI-575 administered at 25.0 mg/kg as a 90-minute IV infusion on Study Day 1 of each 21-day treatment cycle (Q3Wk) until unacceptable toxicity, documentation of disease progression, or other reasons for participant withdrawal occurred.
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MEDI-575 as an IV infusion
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Number of Participants With Adverse Events
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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An adverse event (AE) is any unfavorable and unintended sign, symptom, or disease temporally associated with the use of study drug, whether or not considered related to the study drug.
Treatment-emergent AEs (TEAEs) are events present at baseline that worsened in intensity after administration of study drug or events absent at baseline that emerged after administration of study drug, for the period extending to 30 days after the last dose of study drug.
Participants were counted only once for each event and by the highest event severity, regardless of how many events the participant experienced.
The AEs were summarized using Medical Dictionary for Regulatory Activities (MedDRA) version 14.1.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Number of Participants With Serious Adverse Events
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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A serious AE (SAE) is any AE that results in death, is immediately life threatening, require (or prolong) inpatient hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly or birth defect, or is an important medical event that may jeopardize the participant or may require medical intervention to prevent one of the outcomes listed above.
Treatment-emergent SAEs that emerged after start of study drug were reported.
Participants were counted only once for each event and by the highest event severity, regardless of how many events the participant experienced.
The SAEs were summarized using MedDRA version 14.1.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Treatment-emergent Adverse Events Related to Laboratory Parameters
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Laboratory evaluations of blood and urine samples were performed, including hematology (complete blood count, differential, and platelet count); serum chemistry (SrChem) aspartate transaminase (AST), alanine transaminase, total bilirubin, creatinine, alkaline phosphatase, sodium, potassium, chloride, phosphorus, calcium, glucose, magnesium, albumin, and lactate dehydrogenase); and routine urinalysis.
Number of participants with TEAEs related to laboratory evaluations were reported.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Treatment-emergent Adverse Events Related to Electrocardiogram Evaluations
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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All 12-lead electrocardiograms (ECGs) performed during the study were obtained in triplicate (ie, 3 ECGs were obtained within a 5-minute time interval) and analyzed.
ECG parameters included heart rate (high and low), QT interval, QTcB (corrected QT interval per Bazett's formula), and QTcF (corrected QT interval per Fridericia's formula).
Number of participants with TEAEs related to ECG after the start of study drug were reported.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Treatment-emergent Adverse Events Related to Vital Sign Parameters
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Vital signs (temperature, blood pressure, pulse rate, and respiratory rate) were performed throughout the study.
The TEAEs related to vital signs in participants were reported.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Maximum Tolerated Dose (MTD)
Ramy czasowe: From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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For the dose escalation phase, a minimum of 21 evaluable participants (3 participants each in Dose Cohorts 1 through 7) were required for this study if Dose Limiting Toxicities (DLTs) do not occur.
If a DLT does occur among the first 3 participants in a cohort, 3 additional participants were to be added to the cohort; 3 more participants were to be added to a cohort to determine the MTD if only 3 participants have been previously treated at that dose.
The MTD is the maximum dose at which no more than 1 out of 6 participants experienced a DLT.
A DLT is defined as any grade 3 or higher hematologic toxicity or any grade 3 or higher non-hematologic toxicity except grade 3 fever (in the absence of neutropenia) or grade 3 rigors/chills.
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From the start of study drug administration through 30 days after last dose of MEDI-575, up to 112 weeks
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Pharmacokinetics (PK) of MEDI-575 After the First Dose: Observed Maximum Serum Concentration (Cmax)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The concentration of MEDI-575 quantitatively determined in serum samples using a validated electrochemiluminescence (ECL) PK assay.
The Cmax after the first dose was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
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For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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PK of MEDI-575 After the First Dose: Time to Maximum Concentration (Tmax)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The time to reach maximum serum concentration after the first dose of MEDI-575 was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
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For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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PK of MEDI-575 After the First Dose: Dose-normalized Maximum Serum Concentration (Cmax/Dose)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The Cmax/dose after the first dose of MEDI-575 was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
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For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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PK of MEDI-575 After the First Dose: Trough Serum Concentration (Ctrough)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The Ctrough ie, measured concentration at the end of a dosing interval (taken directly before next dose administration) of MEDI-575 was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
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For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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PK of MEDI-575 After the First Dose: Area Under the Serum Concentration-time Curve Over the Dosing Interval (AUCτ)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The AUCτ was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
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For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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PK of MEDI-575 After the First Dose: Dose-normalized Area Under the Serum Concentration-time Curve (AUCτ/Dose)
Ramy czasowe: For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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The AUCτ/dose was obtained directly from the measured concentration-time curves.
The concentration-time curve is the result of blood sampling at specified time points and its measured concentration of MEDI-575.
|
For 0.5/3, 6, 9, 12, 15 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3 and 8 (pre-dose); For 25 and 35 mg/kg: Cycle 1: Day 1 (pre- and end of infusion, 2 and 6 hours post infusion), Days 2, 3, 8 and 15.
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Number of Participants Positive for Anti-drug Antibodies Formation for MEDI-575 at Any Visit
Ramy czasowe: Preinfusion on Cycle 1 Day 1 and 30 days after the last dose, up to 112 weeks
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Blood samples for immunogenicity assessments were collected from participants prior to the initiation of infusion of each treatment cycle of MEDI-575.
Anti-MEDI-575 antibodies were analyzed using the electro-chemiluminescence (ECL) based method.
Only the number of participants positive for anti-MEDI-575 antibodies at any visit are presented.
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Preinfusion on Cycle 1 Day 1 and 30 days after the last dose, up to 112 weeks
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Percentage of Participants With Objective Response
Ramy czasowe: From study entry through the end of the study, up to 34 months
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Objective response rate is defined as the proportion of participants with confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST) guidelines.
Confirmed responses are those that persist on repeat imaging study at least 4 weeks after the initial documentation of response.
The CR is defined as disappearance of all target and non-target lesions, and normalization of tumor marker level.
The PR is defined as at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
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From study entry through the end of the study, up to 34 months
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Time to Response
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Time to response was measured from the start of treatment with MEDI-575 to the first documentation of objective response (confirmed CR or PR).
The time to response is assessed only for the participants who have achieved the objective response.
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Duration of Response
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Duration of response is defined as the duration from the first documentation of objective response to the first documented disease progression.
Disease progression is defined according to RECIST guidelines (ie, at least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions).
The duration of response was censored on the date of last tumor assessment documenting absence of disease progression for participants who have no documented progression prior to data cutoff, dropout, or the initiation of alternate anticancer treatment.
Duration of response was calculated for the subgroup of participants with an objective response.
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Time to Progression
Ramy czasowe: Start of treatment with MEDI-575 until the documentation of disease progression, up to 24 months
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Time to progression (TTP) is defined as time from the start of treatment with MEDI-575 until the documentation of disease progression.
Disease progression is defined according to RECIST guidelines (ie, at least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions).
The TTP was censored on the date of last tumor assessment documenting absence of tumor progression for participants who have no documented progression prior to data cutoff, dropout, or the initiation of alternate anticancer treatment.
TTP was censored on the first date of treatment for the participants with no tumor assessments after the start of MEDI-575 treatment.
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Start of treatment with MEDI-575 until the documentation of disease progression, up to 24 months
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Progression-free Survival
Ramy czasowe: Start of treatment with MEDI-575 until the documentation of disease progression or death due to any cause whichever occurs first, up to 24 months
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Progression-free survival (PFS) is defined as time from the start of treatment with MEDI-575 until the documentation of disease progression or death due to any cause, whichever occurred first.
Disease progression is defined according to RECIST guidelines (ie, at least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions).
PFS was censored on the date of last tumor assessment documenting absence of tumor progression for participants who have no documented progression and were still alive prior to data cutoff, dropout, or the initiation of alternate anticancer treatment.
PFS was censored on the first date of treatment for the participants with no tumor assessments after the start of MEDI-575 treatment.
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Start of treatment with MEDI-575 until the documentation of disease progression or death due to any cause whichever occurs first, up to 24 months
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Overall Survival
Ramy czasowe: From the start of treatment with MEDI-575 until death or end of study, up to 33 months
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Overall survival (OS) is defined as the time from the start of treatment with MEDI-575 until death.
For the participants who were alive at the end of study or lost to follow-up, OS was censored on the last date when participants were known to be alive.
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From the start of treatment with MEDI-575 until death or end of study, up to 33 months
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Współpracownicy i badacze
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Publikacje i pomocne linki
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Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
2 marca 2009
Zakończenie podstawowe (Rzeczywisty)
19 stycznia 2012
Ukończenie studiów (Rzeczywisty)
19 stycznia 2012
Daty rejestracji na studia
Pierwszy przesłany
23 grudnia 2008
Pierwszy przesłany, który spełnia kryteria kontroli jakości
30 grudnia 2008
Pierwszy wysłany (Oszacować)
1 stycznia 2009
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
26 czerwca 2018
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
3 kwietnia 2018
Ostatnia weryfikacja
1 kwietnia 2018
Więcej informacji
Terminy związane z tym badaniem
Inne numery identyfikacyjne badania
- MI-CP187
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .