Safety Study of MG1102 in Patients With Solid Tumors

Solid Tumors Clinical Trial

Official title:

A PHASE 1, OPEN LABEL, DOSE ESCALATION STUDY TO INVESTIGATE THE SAFETY, TOLERABILITY, AND PHARMACOKINETICS OF MG1102 IN PATIENTS WITH SOLID TUMORS

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01809912
• Other study ID #: MG1102_001
• Status: Terminated
• Phase: Phase 1
• First received: October 30, 2012
• Last updated: November 25, 2015
• Start date: November 2010
• Est. completion date: March 2013

Study information

• Verified date: January 2014
• Source: Green Cross Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationKorea: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

To investigate the safety and tolerability of a 28 day course of intravenous (IV) MG1102 in patients with solid tumors for which no standard therapy is available.

Description:

This is an open-label, Dose Escalation Study, multicenter phase I study to evaluate the safety and tolerability, determine the pharmacokinetics, and obtain preliminary information regarding pharmacodynamics and efficacy of MG1102 in subjects with solid tumor.

Each subject will receive on dose of MG1102 followed by a 6-day rest period. If the initial dose is tolerated, subject will continue with the 21 days of MG1102 administration (5 days on treatment, 2 days off treatment for 3 weeks.) Subjects that have a tumor response as stable disease, may continue therapy on a compassionate use.

Study Duration : for a minimum of 8 weeks

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 16
• Est. completion date: March 2013
• Est. primary completion date: March 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years of age or older

• Solid tumors refractory to conventional therapy or the subject does not tolerate the conventional therapy

• Evaluable disease or at least one measurable tumor mass by a radiographic technique

• Life expectancy =3 months

• Suitable for intravenous administration of study medication

• Signed written informed consent

• Adequate bone marrow, renal, and liver function

• Coagulation profile with aPTT and INR, each = 1.5 x ULN

• No evidence of active Hepatitis B or Hepatitis C infection

• Proteinuria <100 mg

• ECOG performance status =2

• Female subjects must agree to use contraceptive measures

• Negative serum ß-hCG

• Ability and willingness to comply with the study protocol

Exclusion Criteria:

• Pregnant or lactating women

• Therapy with systemic anticoagulant or antithrombotic agentswithin 7 days prior to first dose

• Hemoptysis within 3 months prior to first dose

• Cytotoxic chemotherapy, immunotherapy, or radiotherapy within 4 weeks prior to first dose

• Surgery or visceral biopsy within 28 days prior to first dose

• Minor surgical procedure performed within 7 days prior to first dose

• Prior exposure to MG1102

• Known history of HIV

• With active bacterial infections and/or receiving systemic antibiotics

• Current or past diagnosis of leukemia

• Known CNS metastases or clinical evidence of CNS

• Non-healing wound within past 2 weeks

• Bleeding diathesis or bleeding within 14 days prior to enrollment

• Clinically significant thrombosis

• Non-malignant GI bleeding, gastric stress ulcerations, or peptic ulcer disease

• History of idiopathic or hereditary angioedema

• History of sickle cell or any hemolytic anemia

• Require hemoglobin, WBC, or platelet transfusion support or use of hematopoietic growth factors within 2 weeks prior to entry

• Uncontrolled hypertension

• History of clinically significant renal disease

• History of significant medical illness of cardiac or CNS disease within the past 6 months

• Treatment with an investigational agent within the longest time frame of either 5 half-lives or 30 days of initiating study drug

• Medical or psychiatric illness

• Recreational substance use or psychiatric illness

• Known hypersensitivity to MG1102 or components of the formulation

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Solid Tumors

Intervention

Drug:
• Recombinant human apolipoprotein(a) Kringle V

Locations

Country	Name	City	State
Korea, Republic of	Yonsei Cancer Center, Yonsei University Severance Hospital	Seoul

Sponsors (2)

Lead Sponsor	Collaborator
Green Cross Corporation	ICON Clinical Research

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To investigate the safety and tolerability IV MG1102	Adverse events, physical examinations, vital signs, ECGs, clinical laboratory evaluations, lipid profiles	A minimum of 9 weeks	Yes
Secondary	Each subject's serum drug concentration-time data to determine the pharmacokinetic profile of MG1102		for 25 days	No
Secondary	standard clinical serum tumor markers via serum samples to obtain preliminary information regarding the pharmacodynamics of MG1102		A minimum of 10 weeks	No
Secondary	Determination of response assessed by RECIST v1.1 and Choi criteria to obtain preliminary information regarding the efficacy of MG1102		A minimum of 11 weeks	No