A Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-573 in Subjects With Advanced Solid Tumors
keskiviikko 31. lokakuuta 2018 päivittänyt: MedImmune LLC
A Phase 1, Multicenter, Open-label, Single-arm, Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-573, a Fully Human Monoclonal Antibody Directed Against Insulin-like Growth Factors I and II, in Subjects With Advanced Solid Tumors Refractory to Standard Therapy or for Which No Standard Therapy Exists
Evaluate the safety and tolerability of MEDI-573 in adult subjects with advanced solid tumors refractory to standard therapy or for which no standard therapy exists.
Tutkimuksen yleiskatsaus
Opintotyyppi
Interventio
Ilmoittautuminen (Todellinen)
43
Vaihe
- Vaihe 1
Yhteystiedot ja paikat
Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.
Opiskelupaikat
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Arizona
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Scottsdale, Arizona, Yhdysvallat, 85259
- Research Site
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Florida
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Jacksonville, Florida, Yhdysvallat, 32224
- Research Site
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Massachusetts
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Boston, Massachusetts, Yhdysvallat, 02115
- Research Site
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Michigan
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Detroit, Michigan, Yhdysvallat, 48201
- Research Site
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Minnesota
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Rochester, Minnesota, Yhdysvallat, 55905
- Research Site
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Pennsylvania
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Philadelphia, Pennsylvania, Yhdysvallat, 19111
- Research Site
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Osallistumiskriteerit
Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.
Kelpoisuusvaatimukset
Opintokelpoiset iät
18 vuotta - 99 vuotta (Aikuinen, Vanhempi Aikuinen)
Hyväksyy terveitä vapaaehtoisia
Ei
Sukupuolet, jotka voivat opiskella
Kaikki
Kuvaus
Inclusion Criteria:
- Histologically confirmed advanced solid tumor for which no curative or standard therapies exist.
- Karnofsky Performance Status ≥60.
- Adequate hematological function.
- Adequate organ function.
- Women of non-child-bearing potential (defined as being >1 year post-menopausal) or using effective contraception, e.g., use of oral contraceptives with an additional barrier method (since the investigational product may impair the effectiveness of oral contraceptives), double barrier methods (diaphragm with spermicidal gel or condoms with contraceptive foam), Depo-Provera, partner vasectomy, or total abstinence, from the time the informed consent is signed through 30 days after the last dose of MEDI-573. Male subjects with partners of child-bearing potential must be surgically sterile or use contraceptive method as described above from the time of the initiation of MEDI-573 through 30 days after the last dose of MEDI-573.
Exclusion Criteria:
- No prior treatment within 4 weeks of study drug administration.
- No concurrent therapy for treatment of cancer.
- No uncontrolled 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.
- Documented brain metastasis.
- Pregnancy or lactation or plans to become pregnant while on study.
- Clinically significant abnormality on ECG.
Opintosuunnitelma
Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
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Kokeellinen: MEDI-573 0.5 mg/Kg QWk Dose Escalation
Participants received MEDI-573 0.5 milligram per kilogram (mg/kg) as a 60-minute intravenous (IV) infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 1.5 mg/Kg QWk Dose Escalation
Participants received MEDI-573 1.5 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 5 mg/Kg QWk Dose Escalation
Participants received MEDI-573 5 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 10 mg/Kg QWk Dose Escalation
Participants received MEDI-573 10 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 15 mg/Kg QWk Dose Escalation
Participants received MEDI-573 15 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 30 mg/Kg Q3Wk Dose Escalation
Participants received MEDI-573 30 mg/kg as a 90-minute IV infusion once every 21 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 45 mg/Kg Q3Wk Dose Escalation
Participants received MEDI-573 45 mg/kg as a 90-minute IV infusion once every 21 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 5 mg/Kg QWk Dose Expansion
Participants received MEDI-573 5 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
|
Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Kokeellinen: MEDI-573 15 mg/Kg QWk Dose Expansion
Participants received MEDI-573 15 mg/kg as a 60-minute IV infusion once every 7 days until unacceptable toxicity, documentation of disease progression, or other reason for participant withdrawal.
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Administered at a dose determined by the subject's enrollment cohort as an IV infusion as part of a 21 day treatment cycle.
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (SAEs)
Aikaikkuna: From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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AEs were any unfavorable and unintended signs (including abnormal laboratory findings), symptoms, or diseases temporally associated with the use of MEDI-573, whether or not considered related to MEDI-573.
A SAE was any AE that resulted in: death; inpatient hospitalization or prolongation of existing hospitalization; persistent or significant disability or incapacity; was life-threatening; was a congenital anomaly/birth defect in the offspring of a study participant; or was an important medical event that may not have resulted in death, threatened life, or required hospitalization and that, based on appropriate medical judgment, may have jeopardized the participant and may have required medical or surgical intervention to prevent one of the outcomes above.
TEAEs were defined as AEs present at baseline that worsened in intensity after administration of MEDI-573, or events absent at baseline that emerged after administration of MEDI-573, up to 30 days after the last dose.
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From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Number of Participants With Clinical Laboratory Abnormalities Reported as TEAEs
Aikaikkuna: From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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An abnormal laboratory finding that was judged by the investigator to be medically significant was reported as an AE.
TEAEs were defined as events present at baseline that worsened in intensity after administration of MEDI-573, or events absent at baseline that emerged after administration of MEDI-573, for the period extending to 30 days after the last dose.
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From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Number of Participants With Vital Signs and Physical Findings Abnormalities Reported as TEAEs
Aikaikkuna: From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Vital signs and physical findings included parameters such as heart rate, blood pressure, temperature, and respiratory rate.
TEAEs were defined as events present at baseline that worsened in intensity after administration of MEDI-573 or events absent at baseline that emerged after administration of MEDI-573, for the period extending to 30 days after the last dose.
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From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Maximum Tolerated Dose (MTD) of MEDI-573
Aikaikkuna: Cycle 1 Day 1 through Cycle 1 Day 21
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The MTD was defined as the highest dose that can be safely administered to participants and was determined by the number of participants in each cohort with a dose-limiting toxicity (DLT).
The number and proportion of participants in each dose cohort and the number of participants with a DLT was presented using the total number of participants in the MTD Evaluable Population as the denominator.
2 participants from Cohorts 0.5 and 5 mg/kg QWk (1 in each cohort) did not complete the DLT period and therefore not evaluable for MTD.
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Cycle 1 Day 1 through Cycle 1 Day 21
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Number of Participants With Dose-Limiting Toxicities (DLTs)
Aikaikkuna: Cycle 1 Day 1 through Cycle 1 Day 21
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A DLT was defined as any grade greater than or equal to (>=) 3 treatment-related non-hematologic toxicity that occurred during the DLT assessment period with the following exceptions: Grade less than (<) 4 serum-high glucose (fasting) with duration of < 24 hours; Grade 3 fever (in the absence of neutropenia) defined as > 40.0 degree centigrade (°C) [greater than (>) 104.0°F] that resolved to normal or baseline within 24 hours of treatment and was not considered an SAE; or Grade 3 rigors/chills that responded to optimal therapy; any Grade >= 3 treatment-related hematologic toxicity that occurred during the DLT assessment period.
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Cycle 1 Day 1 through Cycle 1 Day 21
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Optimal Biologically Effective Dose (OBED) of MEDI-573
Aikaikkuna: From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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The OBED was defined as the dose at which all circulating insulin-like growth factor (IGF)-1 and IGF-2 ligand was sequestered by MEDI-573.
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From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Maximum Observed Serum Concentration (Cmax) After the First Dose
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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The Cmax was the maximum observed serum concentration of MEDI-573.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Time to Reach Maximum Observed Concentration (Tmax) After the First Dose
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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The tmax was defined as actual sampling time to reach the maximum observed serum concentration of MEDI-573.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Trough Serum Concentration (Ctrough) After the First Dose
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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The Ctrough was the lowest serum concentration of MEDI-573 within a dosing interval.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Dose Normalized Cmax (Cmax/Dose) After the First Dose
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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The Cmax/dose was the dose-normalized maximum serum concentration of MEDI-573.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Area Under the Serum Concentration-time Curve Over the First Dosing Interval (AUCτ)
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Area under the serum concentration-time curve over the first dosing interval.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Dose-normalized Area Under the Serum Concentration Time Curve Over the First Dosing Interval (AUCτ/Dose)
Aikaikkuna: For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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The AUCtau/dose was a measure of dose-normalized area under the serum concentration-time curve over the first dosing interval.
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For weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); For 3 weekly dosing: Pre- and post-infusion (0, 2, 6, 24, and 48 hours post-infusion); and on Days 8 and 15
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Number of Participants With Positive Anti-Drug Antibodies (ADA) to MEDI-573
Aikaikkuna: Pre-infusion on Day 1 of each cycle, end of treatment, and 90 days after last dose MEDI-573 (up to 3.5 years)
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Two methods were used to assess the immunogenicity data: an ECL-based method and measurement of neutralizing ADA.
The titer was calculated by multiplying the minimum assay dilution factor by the reciprocal of the highest dilution factor which yielded an ECL multiple equal to or greater than the screening assay cut-point factor.
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Pre-infusion on Day 1 of each cycle, end of treatment, and 90 days after last dose MEDI-573 (up to 3.5 years)
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Objective Response Rate (ORR)
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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The ORR was defined as the proportion of participants with confirmed complete response (CR) or partial response (PR) according to the RECIST criteria The CR was defined as disappearance of all target and nontarget lesions and no new lesions; and PR was definded as >= 30% decrease in the sum of diameters of Target Lesions (compared to baseline [screening]) and no new lesions.
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From study entry through the end of the study, up to 3.5 years
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Progression-free Survival (PFS)
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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Progression-free survival (PFS) was defined as the duration from the start of treatment with MEDI-573 until the documentation of disease progression or death due to any cause, whichever occurred first.
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From study entry through the end of the study, up to 3.5 years
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Time to Progression
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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Time to disease progression (TTP) was defined as the duration from the start of treatment with MEDI-573 until the documentation of disease progression.
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From study entry through the end of the study, up to 3.5 years
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Overall Survival
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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Overall survival (OS) was defined as the time from the start of treatment with MEDI-573 until death.
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From study entry through the end of the study, up to 3.5 years
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Time to Response (TTR)
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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Time to response was defined as the duration from the start of treatment with MEDI-573 to the first documentation of objective response (confirmed CR or PR) and was only assessed in participants who had achieved objective response.
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From study entry through the end of the study, up to 3.5 years
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Duration of Response
Aikaikkuna: From study entry through the end of the study, up to 3.5 years
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Duration of response was defined as the duration from the first documentation of objective response (confirmed CR or PR) to the first documented disease progression.
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From study entry through the end of the study, up to 3.5 years
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Suppression Profiles of IGF-I and IGF-II Post-Administration of MEDI-573
Aikaikkuna: From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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The suppression profiles of both IGF-1 and IGF-2 post administration of MEDI-573 in relation to time course of antibody concentrations in serum were evaluated during treatment.
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From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years
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Yhteistyökumppanit ja tutkijat
Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.
Sponsori
Tutkijat
- Opintojohtaja: Susan Perez, MD, MSc, MedImmune LLC
Julkaisuja ja hyödyllisiä linkkejä
Tutkimusta koskevien tietojen syöttämisestä vastaava henkilö toimittaa nämä julkaisut vapaaehtoisesti. Nämä voivat koskea mitä tahansa tutkimukseen liittyvää.
Hyödyllisiä linkkejä
Opintojen ennätyspäivät
Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan julkisella verkkosivustolla.
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Maanantai 9. maaliskuuta 2009
Ensisijainen valmistuminen (Todellinen)
Tiistai 11. syyskuuta 2012
Opintojen valmistuminen (Todellinen)
Tiistai 11. syyskuuta 2012
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Tiistai 23. joulukuuta 2008
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Tiistai 30. joulukuuta 2008
Ensimmäinen Lähetetty (Arvio)
Torstai 1. tammikuuta 2009
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Maanantai 4. maaliskuuta 2019
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Keskiviikko 31. lokakuuta 2018
Viimeksi vahvistettu
Maanantai 1. lokakuuta 2018
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