A Pharmacokinetic Study of AMG 386 in Cancer Subjects With Normal and Impaired Renal Function

Advanced Solid Tumors Clinical Trial

Official title:

An Open-label Pharmacokinetic Study of AMG 386 in Advanced Cancer Subjects With Normal and Impaired Renal Function

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01331941
• Other study ID #: 20090277
• Status: Completed
• Phase: Phase 1
• First received: March 24, 2011
• Last updated: November 1, 2017
• Start date: September 19, 2011

Study information

• Verified date: November 2017
• Source: Amgen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 1, open-label pharmacokinetic study where up to 40 subjects with advanced solid tumors (up to 6-10 with normal renal function and up to 18-30 with varying degrees of renal dysfunction) will receive weekly doses of AMG 386 intravenously. The primary objective is to evaluate the pharmacokinetics (PK) of single agent AMG 386 in subjects with various degrees of renal function. Once the AMG 386 PK characterization is complete in the first 5 weeks of the study, all subjects will be allowed to continue to receive AMG 386 weekly only or subjects in group 1, 2 or 3 can opt to receive AMG 386 weekly in combination with paclitaxel until disease progression, unacceptable toxicity or withdrawal of consent.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. primary completion date: February 26, 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Men or women = 18 years of age

• Must have a pathologically documented, and definitively diagnosed, advanced solid tumor that is refractory to standard treatment, or for which no curative therapy is available, or for subjects who refuse standard therapy

• Evaluable OR measurable disease by RECIST 1.1 criteria

• Eastern Cooperative Oncology Group (ECOG) performance status = 1

• Life expectancy of > 3 months, in the opinion of and as documented by the investigator

• Subject or subject's legally acceptable representative has provided informed consent

Exclusion Criteria:

• Subjects with gastric cancer or any malignancy with purely squamous cell histology

• Known history of primary central nervous system (CNS) tumors or CNS metastases

• Myocardial infarction within 1 year before study day 1, unstable or uncontrolled disease/condition related to or affecting cardiac function (eg, unstable angina, congestive heart failure, New York Heart Association > class II, uncontrolled hypertension [diastolic > 90 mmHg; systolic > 150 mmHg in repeated measurements])

• History of stroke, arterial or venous thrombosis, or pulmonary embolism within 1 year before study day 1

• Active grade 2 or greater peripheral vascular disease or peripheral edema

• History of interstitial lung disease (eg, pneumonitis or pulmonary fibrosis)

• Non-healing wound, ulcer (including gastrointestinal) or fracture

• Known positive test for human immunodeficiency virus infection, or active hepatitis B or hepatitis C infection

• Major surgery within 4 weeks before study day 1

• Absolute neutrophils count (ANC) < 1.0 x 10^9/L; or platelet count < 100 x 10^9/L; or hemoglobin < 9 g/dL; or PTT / aPTT > 1.5 x institutional upper limit of normal (ULN) ); or INR > 1.5

• Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2.5 x ULN (> 5.0 x ULN if liver metastases present)

• Alkaline phosphatase > 2.5 x ULN (> 5.0 x ULN if attributable to liver or bone metastasis)

• Total bilirubin > 1.5 x ULN

• Other investigational procedures during the study

• Previous anti-cancer therapy or investigational agent within 4 weeks prior to study day 1

• Anticoagulation therapy within 4 weeks of study day 1 and while on study (except low dose warfarin (= 2 mg/kg) for prophylaxis against central venous catheter thrombosis)

• Men and women of reproductive potential, unwilling to practice a highly effective method of birth control for the duration of the study and an additional 6 months after the last dose of AMG 386. Highly effective methods of birth control include sexual abstinence (men, women); vasectomy or a condom with spermicide (men) in combination with barrier methods, hormonal birth control or IUD (women).

• Women who are lactating/breastfeeding.

• Women with a positive pregnancy test.

Related Conditions & MeSH terms

• Advanced Solid Tumors
• Kidney Disease
• Kidney Diseases
• Renal Impairment
• Renal Insufficiency

Intervention

Drug:
• AMG 386 + Paclitaxel
15 mg/kg IV (in the vein) of AMG 386 weekly + 80 mg/m^2 IV (in the vein) 3 weeks on/1 week off, optional beginning week 6 until progression, unacceptable toxicity, or withdrawal of consent.
• AMG 386
15 mg/kg IV (in the vein) weekly beginning week 1 day 1 until progression, unacceptable toxicity, or withdrawal of consent.

Locations

Country	Name	City	State
United States	Research Site	Atlanta	Georgia
United States	Research Site	Chicago	Illinois
United States	Research Site	Cleveland	Ohio
United States	Research Site	Lebanon	New Hampshire

Sponsors (1)

Lead Sponsor	Collaborator
Amgen

Country where clinical trial is conducted

United States, 

References & Publications (1)

Wu B, Lewis LD, Harvey RD, Rasmussen E, Gamelin E, Sun YN, Friberg G, Koyner JL, Dowlati A, Maitland ML. A Pharmacokinetic and Safety Study of Trebananib, an Fc-Fusion Peptibody, in Patients With Advanced Solid Tumors and Varying Degrees of Renal Dysfunction. Clin Pharmacol Ther. 2017 Aug;102(2):313-320. doi: 10.1002/cpt.617. Epub 2017 Jun 9. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under the serum concentration-time curve (AUC)		Week 1-5.
Primary	Maximum observed concentration (Cmax)		Week 1-5.
Primary	Time to maximum concentration (tmax)		Week 1-5.
Primary	Minimum observed concentration (Cmin)		Week 1-5.
Primary	Clearance (CL) of AMG 386 calculated as dose divided by AUC on week 5.		Week 1-5
Secondary	Adverse events as a measure of safety		Weekly at each visit AMG 386 is administered, on day 30, 31 and 32 when only PK assessments are scheduled up to and including the last study visit 30 days after the last AMG 386 administration.
Secondary	Changes in vital signs as a measure of safety		Weekly at each visit AMG 386 is administered up to and including the last study visit 30 days after the last AMG 386 administration.
Secondary	Changes in clinical laboratory tests as a measure of safety		Weekly from week 1-9 then every 4 weeks thereafter including the last study visit 30 days after the last AMG 386 administration.
Secondary	Anti-AMG 386 antibody formation		Week 1, week 5, week 9 and every 16 weeks thereafter including the last study visit 30 days after the last AMG 386 administration.
Secondary	Tumor objective response measured by CT or MRI (without Gadolinium contrast agents) and assessed by RECIST 1.1 criteria.		Week 5 and every 8 weeks thereafter until the subject's end of participation in the study.

External Links

•   AmgenTrials clinical trials website