A Dose-escalation Study to Evaluate the Safety, Tolerability, and Antitumor Activity of MEDI-573 in Subjects With Advanced Solid Tumors

Phase 1

Completed

Conditions: Cancer

Interventions: Drug: MEDI-573

Registration Number: NCT00816361

Lead Sponsor: MedImmune LLC

Brief Summary: 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.

Detailed Description: Not available

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 43

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.

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
MEDI-573 45 mg/Kg Q3Wk Dose Escalation	MEDI-573	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.
MEDI-573 5 mg/Kg QWk Dose Escalation	MEDI-573	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.
MEDI-573 15 mg/Kg QWk Dose Escalation	MEDI-573	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.
MEDI-573 10 mg/Kg QWk Dose Escalation	MEDI-573	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.
MEDI-573 15 mg/Kg QWk Dose Expansion	MEDI-573	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.
MEDI-573 30 mg/Kg Q3Wk Dose Escalation	MEDI-573	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.
MEDI-573 0.5 mg/Kg QWk Dose Escalation	MEDI-573	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.
MEDI-573 5 mg/Kg QWk Dose Expansion	MEDI-573	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.
MEDI-573 1.5 mg/Kg QWk Dose Escalation	MEDI-573	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.

Primary Outcome Measures

Name	Time	Method
Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (SAEs)	From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years	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.
Number of Participants With Clinical Laboratory Abnormalities Reported as TEAEs	From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years	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.
Number of Participants With Vital Signs and Physical Findings Abnormalities Reported as TEAEs	From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years	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.
Maximum Tolerated Dose (MTD) of MEDI-573	Cycle 1 Day 1 through Cycle 1 Day 21	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.
Number of Participants With Dose-Limiting Toxicities (DLTs)	Cycle 1 Day 1 through Cycle 1 Day 21	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.
Optimal Biologically Effective Dose (OBED) of MEDI-573	From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years	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.

Secondary Outcome Measures

Name	Time	Method
Dose Normalized Cmax (Cmax/Dose) After the First Dose	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	The Cmax/dose was the dose-normalized maximum serum concentration of MEDI-573.
Area Under the Serum Concentration-time Curve Over the First Dosing Interval (AUCτ)	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	Area under the serum concentration-time curve over the first dosing interval.
Maximum Observed Serum Concentration (Cmax) After the First Dose	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	The Cmax was the maximum observed serum concentration of MEDI-573.
Time to Reach Maximum Observed Concentration (Tmax) After the First Dose	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	The tmax was defined as actual sampling time to reach the maximum observed serum concentration of MEDI-573.
Trough Serum Concentration (Ctrough) After the First Dose	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	The Ctrough was the lowest serum concentration of MEDI-573 within a dosing interval.
Dose-normalized Area Under the Serum Concentration Time Curve Over the First Dosing Interval (AUCτ/Dose)	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	The AUCtau/dose was a measure of dose-normalized area under the serum concentration-time curve over the first dosing interval.
Number of Participants With Positive Anti-Drug Antibodies (ADA) to MEDI-573	Pre-infusion on Day 1 of each cycle, end of treatment, and 90 days after last dose MEDI-573 (up to 3.5 years)	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.
Objective Response Rate (ORR)	From study entry through the end of the study, up to 3.5 years	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.
Progression-free Survival (PFS)	From study entry through the end of the study, up to 3.5 years	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.
Time to Progression	From study entry through the end of the study, up to 3.5 years	Time to disease progression (TTP) was defined as the duration from the start of treatment with MEDI-573 until the documentation of disease progression.
Overall Survival	From study entry through the end of the study, up to 3.5 years	Overall survival (OS) was defined as the time from the start of treatment with MEDI-573 until death.
Time to Response (TTR)	From study entry through the end of the study, up to 3.5 years	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.
Duration of Response	From study entry through the end of the study, up to 3.5 years	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.
Suppression Profiles of IGF-I and IGF-II Post-Administration of MEDI-573	From the start of study treatment through 30 days after the last dose of MEDI-573, up to 3.5 years	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.