Tissue Procurement Substudy for Participants in Study CP-MGA271-01

Sponsor
MacroGenics (Industry)
Overall Status
Terminated
CT.gov ID
NCT01918930
Collaborator
Massachusetts General Hospital (Other)
6
7
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39
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Study Details

Study Description

Brief Summary

The purpose of this study is to gain a better understanding about how the study drug MGA271 works. No test drug will be given in this study. Patients with easily accessible tumors at the screening visit for participation in Study CP-MGA271-01 will be asked to participate in this substudy. Patients will undergo two excisional biopsies, punch biopsies, or core needle biopsies.

Condition or Disease Intervention/Treatment Phase
  • Biological: MGA271
Phase 1

Detailed Description

Patients with easily accessible tumors (generally, metastatic deposits involving skin, subcutaneous tissues, or peripheral lymph node whose excision would not require general anaesthesia or the invasion of a body cavity) at the screening visit for participation in Study CP-MGA271-01 (the main study) will be asked to participate in this substudy. After providing appropriate informed consent, patients will undergo excisional biopsy, punch biopsy, or core needle biopsy of the accessible tumor prior to receiving study drug in the main study and then again after the first cycle of study drug is completed.

Some of the biopsy tissue will be sent to a central laboratory for research purposes. The central lab will analyze the tissue to see what effects that the study drug might have on tumors.

Study Design

Study Type:
Interventional
Actual Enrollment :
6 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
A Tissue Procurement and Examination Substudy of Study CP-MGA271-01 (NCT01391143)
Study Start Date :
Jul 1, 2013
Actual Primary Completion Date :
Oct 1, 2016
Actual Study Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: MGA271

MGA271 (administered in main study CP-MGA271-01)

Biological: MGA271
MGA271 anti-B7-H3 monoclonal antibody

Outcome Measures

Primary Outcome Measures

  1. Mechanism of Action [up to 50 days]

    Exploratory analyses from immunohistochemistry (IHC) and flow cytometry testing to determine the effect of MGA271 on tumor cells.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Qualified, by meeting all inclusion and exclusion criteria, for participation in Study CP-MGA271-01.

  • Must have provided informed consent to participate in Study CP-MGA271-01.

  • Must have accessible tumors (generally speaking, metastatic deposits involving skin, subcutaneous tissue, or peripheral lymph node whose excision, punch biopsy, or core needle biopsy would not require general anaesthesia or the invasion of a body cavity).

  • Willing to undergo two minor surgical procedures with no expectation of personal benefit

  • Have provided Informed Consent for this substudy as indicated by a signature on an approved consent document obtained from the patient or his/her legally authorized representative

Exclusion Criteria:
  • Any medical condition that would contraindicate the use of local or locoregional anaesthesia, or conscious sedation for the intended minor surgical procedure.

  • Any medical condition (eg. skin disease or bleeding diathesis) that would hinder wound healing following a minor surgical procedure.

  • Dementia or altered mental status that would preclude understanding and rendering of informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCLA Hematology-Oncology Clinic Los Angeles California United States 90095
2 Moffitt Cancer Center Tampa Florida United States 33612
3 The University of Chicago Chicago Illinois United States 60637
4 Massachusetts General Hospital Cancer Center Boston Massachusetts United States 02114
5 Carolina BioOncology Institute Huntersville North Carolina United States 28078
6 Hospital of the University of Pennsylvania/Abramson Cancer Center Philadelphia Pennsylvania United States 19104
7 Sarah Cannon Research Institute Nashville Tennessee United States 37203

Sponsors and Collaborators

  • MacroGenics
  • Massachusetts General Hospital

Investigators

  • Study Director: Chief Medical Officer, MacroGenics

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
MacroGenics
ClinicalTrials.gov Identifier:
NCT01918930
Other Study ID Numbers:
  • CP-MGA271-01a
First Posted:
Aug 8, 2013
Last Update Posted:
Feb 8, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by MacroGenics
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 8, 2022