Sym013 (Pan-HER) in Patients With Advanced Epithelial Malignancies

Oncology Clinical Trial

Official title:

An Open-label, Multicenter, Phase 1a/2a Trial Investigating the Safety, Tolerability and Antitumor Activity of Multiple Doses of Sym013, a mAb Mixture Targeting EGFR, HER2 and HER3, in Patients With Advanced Epithelial Malignancies

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02906670
• Other study ID #: Sym013-01
• Status: Terminated
• Phase: Phase 1/Phase 2
• Start date: November 1, 2016
• Est. completion date: June 2019

Study information

• Verified date: August 2020
• Source: Symphogen A/S
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is the first study to test Sym013 (Pan-HER) in humans. The primary purpose of this study is to see if Sym013 is safe and effective for patients with advanced epithelial malignancies without available therapeutic options.

Description:

This is an open-label, multicenter trial composed of 2 parts in which Sym013 will be evaluated when administered by intravenous infusion in patients with advanced epithelial malignancies without available therapeutic options.

Part 1 is a Phase 1a dose-escalation evaluating weekly (Q1W) and every second week (Q2W) schedules of administration in separate dose-escalation cohorts to determine the recommended phase 2 dose (RP2D) and regimen of Sym013.

Part 2 is a Phase 2a dose-expansion at the RP2D and regimen. Four (4) dose-expansion cohorts will be evaluated in this part of the trial and will be selected based upon findings from Part 1, additional preclinical data, and additional clinical data available at that time from other agents inhibiting these targets. Patients will be entered, depending upon either a defined molecular profile or profiles, or their underlying malignancy, to 1 of 4 corresponding expansion cohorts: Cohort A, Cohort B, Cohort C, or Cohort D.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 32
• Est. completion date: June 2019
• Est. primary completion date: June 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Main inclusion criteria all patients, Part 1 and Part 2:

• Male or female, at least 18 years of age at the time of informed consent

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1

• Life expectancy >3 months assessed during Screening

• Documented (histologically- or cytologically-proven) epithelial malignancy that is locally advanced or metastatic, having received all therapy known to confer clinical benefit

Additional inclusion criteria applicable to Part 2 ONLY:

• Epithelial malignancy (tumor types to be determined), measurable according to RECIST v1.1 that has been confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) within 4 weeks prior to C1/D1

• Willingness to undergo a pre-and post-dosing biopsy (total of 2 biopsies) from primary or metastatic tumor site(s) considered safe for biopsy

Exclusion Criteria:

• Any antineoplastic agent for the primary malignancy (standard or investigational) without delayed toxicity within 4 weeks or 5 plasma half-lives (whichever is shortest) prior to C1/D1, except nitrosoureas and mitomycin C within 6 weeks prior to C1/D1.

• Part 2 ONLY: Radiotherapy against target lesions within 4 weeks prior to C1/D1, unless there is documented progression of the lesion following radiotherapy

• Immunosuppressive or systemic hormonal therapy (>10 mg daily prednisone equivalent) within 2 weeks prior to C1/D1 with exceptions

• Use of hematopoietic growth factors within 2 weeks prior to C1/D1

• Active second malignancy or history of another malignancy within the last 3 years, with allowed exceptions

• Central nervous system (CNS) malignancies including:

1. Primary malignancies of the CNS

2. Known, untreated CNS or leptomeningeal metastases, or spinal cord compression; patients with any of these not controlled by prior surgery or radiotherapy, or symptoms suggesting CNS metastatic involvement for which treatment is required

• Inadequate recovery from an acute toxicity associated with any prior antineoplastic therapy

• Major surgical procedure within 4 weeks prior to C1/D1 or inadequate recovery from any prior surgical procedure

• Non-healing wounds on any part of the body

• Active thrombosis, or a history of deep vein thrombosis or pulmonary embolism, within 4 weeks prior to C1/D1, unless adequately treated and stable

• Active uncontrolled bleeding or a known bleeding diathesis

• Significant gastrointestinal abnormalities

• Significant cardiovascular disease or condition

• Abnormal hematologic, renal or hepatic function

Related Conditions & MeSH terms

• Neoplasms
• Oncology

Intervention

Drug:
• Sym013
Sym013 is a recombinant antibody mixture containing 6 humanized immunoglobulin G1 (IgG1) monoclonal antibodies (mAbs), which bind specifically to non-overlapping epitopes or domains on the epidermal growth factor receptor (EGFR), and the human epidermal growth factor receptors (HER) HER2 and HER3.

Locations

Country	Name	City	State
United States	Vanderbilt University Medical Center	Nashville	Tennessee
United States	NEXT Oncology	San Antonio	Texas
United States	South Texas Accelerated Research Therapeutics, LLC	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Symphogen A/S

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Part 1: Assess the Safety and Tolerability of Sym013 When Administered Either Q1W or Q2W to Separate Dose-escalation Cohorts of Patients.	Assess the occurrence of dose-limiting toxicities (DLTs) during Cycle 1 of Sym013 administration.	24 months
Primary	Part 2: Evaluate the Antitumor Effect of Sym013 When Administered at the RP2D and Regimen to Patients.	No data were collected for this Outcome Measures as Part 2 of the trial was never initiated.	24 months
Secondary	Part 1: Determine the RP2D and Regimen of Sym013.	No RP2D or regimen of Sym013 was determined as the trial was prematurely terminated	24 months
Secondary	Parts 1 and 2: Evaluate the Immunogenicity of Sym013.	Serum sampling to assess the potential for anti-drug antibody (ADA) formation was not analyzed as the trial was prematurely terminated	42 months
Secondary	Parts 1 and 2: Area Under the Concentration-time Curve Extrapolated to Infinity (AUC).	Will be estimated using non-compartmental methods and actual time points.	0, 2, 4, 8, 24, 48, 168 hours and 336 hours if Q2W
Secondary	Parts 1 and 2: Maximum Concentration (Cmax) and Trough Concentration (Ctrough) - Mean Values.	Will be derived from observed data.	0, 2, 4, 8, 24, 48, 168 hours and 336 hours if Q2W
Secondary	Parts 1 and 2: Time to Reach Maximum Concentration (Tmax).	Will be derived from observed data. End of infusion was defined as time zero (0)	0, 2, 4, 8, 24, 48, 168 hours and 336 hours if Q2W
Secondary	Parts 1 and 2: Elimination Half-life (T½).	Will be estimated using non-compartmental methods and actual time points	0, 2, 4, 8, 24, 48, 168 hours and 336 hours if Q2W
Secondary	Parts 1 and 2: Clearance (CL).	Will be estimated using non-compartmental methods and actual time points.	0, 2, 4, 8, 24, 48, 168 hours and 336 hours if Q2W