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Metastatic Adenocarcinoma of the Colon or RectumPhase 1NCT01765790

Phase 1 Study of Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody in Solid Tumors

A Phase 1 study testing Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody in people with Metastatic Adenocarcinoma of the Colon or Rectum and Malignant Solid Tumors, run by Baxalta now part of Shire at 5 sites in 2 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of the study is to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of anti-MIF antibody in subjects with malignant solid tumors (Arm 1) and in subjects with metastatic adenocarcinoma of the colon or rectum (Arm 2). Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
68 participants
Where
5 sitesin 2 countries
Study dates
14 Jun 2012to 28 Jul 2016
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Main Inclusion Criteria:

  • Males and females 18 years of age and older at the time of screening
  • Anticipated life expectancy > 3 months at the time of screening
  • Arm 1 only: Histologically confirmed malignant solid tumor which is refractory to or has failed standard treatments, or participant is not considered medically suitable to receive standard of care treatment or refuses standard of care treatment
  • Arm 2 only: Histologically or cytologically confirmed diagnosis of metastatic adenocarcinoma of the colon or rectum which is refractory to or has failed standard treatments, or participant is not considered medically suitable to receive standard of care treatment or refuses standard of care treatment
  • Measurable or evaluable disease (as defined in the study protocol)
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1
  • Adequate hematological function (as defined in the study protocol)
  • Adequate renal function (as defined in the study protocol)
  • Adequate liver function (as defined in the study protocol)
  • Adequate venous access
  • Arm 2 only: At least 1 tumor that is amenable to biopsy, as determined by the investigator, and participant must be willing to undergo a biopsy prior to and at least once following anti-macrophage migration inhibitory factor (anti-MIF) antibody treatment
  • For women of childbearing potential, the participant must have a negative pregnancy test at screening and must agree to employ 2 forms of adequate contraceptive measures
  • For males, participants must agree to use adequate contraceptive measures including at least 1 barrier method, and abstain from sperm donation throughout the course of the study and for at least 90 days after the last administration of investigational product.
  • Participant is willing and able to comply with the requirements of the protocol

Main Exclusion Criteria:

  • Known brain tumors or Central nervous system (CNS) metastases
  • Myocardial infarction within 6 months of anti-MIF antibody administration, congestive heart failure (New York Heart Association Class III or Class IV), unstable angina, unstable cardiac arrhythmia requiring medication, or risk factors for polymorphic ventricular tachycardia
  • Uncontrolled hypertension
  • Left ventricular ejection fraction (LVEF) <40%, as determined by screening echocardiogram (echocardiogram results obtained within 90 days prior to screening are acceptable)
  • QT/QTc interval >450 msec, as determined by screening electrocardiogram (ECG)
  • Antitumor therapy (chemotherapy, radiotherapy, antibody therapy, molecular targeted therapy, retinoid therapy, or hormonal therapy) within 4 weeks prior to administration of the investigational product (IP) (6 weeks for nitrosoureas and mitomycin C). Any previous treatment-related toxicities must have recovered to Grade ≤ 1 (graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.03). Prior and concurrent use of hormone deprivation therapies for hormone-refractory prostate cancer or breast cancer are permitted.
  • Major surgery within 4 weeks prior to IP administration
  • Active joint inflammation or history of inflammatory arthritis or other immune disorder involving the joints
  • Active infection requiring IV antibiotics within 2 weeks prior to screening
  • Known history of hepatitis B virus (HBV), hepatitis C virus (HCV), or active tuberculosis. Known history of human immunodeficiency virus (HIV) type 1/2 or other immunodeficiency disease.
  • Participant has received a live vaccine within 4 weeks prior to screening
  • Known hypersensitivity to any component of recombinant protein production by Chinese Hamster Ovary (CHO) cells
  • Participant has been exposed to an investigational product (IP) or investigational device in another clinical study within 4 weeks prior to IP administration, or is scheduled to participate in another clinical study involving an IP or investigational device during the course of this study
  • Participant is nursing or intends to begin nursing during the course of the study
  • Any disorder or disease, or clinically significant abnormality on laboratory or other clinical test(s), that in medical judgment may impede the participant's participation in the study, pose increased risk to the participant, or confound the results of the study
  • Participant is a family member or employee of the investigator

Trial locations and contacts

5 sites in 2 countries.

5 sites in 2 countries

United States4 sites
  • Department of Investigator Cancer Therapeutics, University of Texas, MD Anderson Cancer Center

    Houston, Texas, 77030

  • Cancer Therapy and Research Center (CTRC), The University of Texas Health Science Center at San Antonio

    San Antonio, Texas, 78229

  • Florida Cancer Specialists / Sarah Cannon Research Institute

    Sarasota, Florida, 34232

  • Scottsdale Healthcare

    Scottsdale, Arizona, 85258

Other trials in United States

Germany1 site
  • Nationales Centrum für Tumorerkrankungen (NCT) Heidelberg

    Heidelberg, 69120

Other trials in Germany

About this study

Official title: A Phase 1 Open-Label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Anti-MIF Antibody in Subjects With Malignant Solid Tumors

The purpose of the study is to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of anti-MIF antibody in subjects with malignant solid tumors (Arm 1) and in subjects with metastatic adenocarcinoma of the colon or rectum (Arm 2).

Being tested
Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody
Medical subject headings
Colonic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) AntibodyBiological

    • Dosing every 2 weeks
    • Intravenous injection
  • Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) AntibodyBiological

    • Dosing weekly
    • Intravenous injection
Study groups in NCT01765790
Study groupRoleWhat they receive
Malignant Solid Tumor (Arm 1)ExperimentalDose Escalation Phase- Standard dose escalation of anti-MIF antibody in 5 dose groups of 3-6 participants each according to 3+3 design: 1. Dose escalation will be performed after safety data review, following completion of dosing of each cohort. -> 2. Safety data review. If dose escalation permissible -> 3. Next dose group -> 4. Safety data review, etc. Dose Expansion Phase- Enrollment of up to 6 participants to receive anti-MIF antibody (at the maximum tolerated dose or lower) in order to gain further experience with the investigational product at a specific dose level(s).
Receives: Biological: Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody
Metastatic Adenocarcinoma of the Colon or Rectum (Arm 2)ExperimentalDose Escalation Phase- Standard dose escalation of anti-MIF antibody in 3 dose groups of 3-6 participants each according to 3+3 design: 1. Dose escalation will be performed after safety data review, following completion of dosing of each cohort. -> 2. Safety data review. If dose escalation permissible -> 3. Next dose group -> 4. Safety data review, etc. Dose Expansion Phase- Enrollment of up to 6 participants to receive anti-MIF antibody (at the maximum tolerated dose or lower) in order to gain further experience with the investigational product at a specific dose level(s).
Receives: Biological: Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of participants experiencing serious adverse events (SAEs) and/or adverse events (AEs) regardless of causality

    Measured: 14 months

Secondary outcomes (12)
  1. Plasma pharmacokinetic parameters

    Maximum concentration (Cmax), minimum concentration (Cmin), area under the concentration vs time curve (AUC), half-life [t½], clearance (CL), mean residence time (MRT) and volume of distribution at steady state (VDss)

    Measured: 28 days

  2. Tumor response

    Measured: 14 months

  3. Levels of free active MIF and free total MIF in plasma and tumor tissue (where applicable)

    Measured: 14 months

  4. Change in levels of tumor-associated biomarkers, if applicable based on cancer type, following treatment with anti-MIF antibody

    Measured: 14 months

  5. Number of serious adverse events (SAEs) and/or adverse events (AEs), regardless of causality

    Measured: 14 Months

  6. Number of participants experiencing related serious adverse events (SAEs) and/or adverse events (AEs)

    Measured: 14 months

  7. Number of related serious adverse events (SAEs) and/or adverse events (AEs)

    Measured: 14 months

  8. Number of dose limiting toxicities (DLTs)

    Measured: 14 months

  9. Number of participants experiencing dose limiting toxicity (DLT)

    Measured: 14 months

  10. Number of participants who develop binding and/or neutralizing anti-anti-macrophage migration inhibitory factor (anti-MIF) antibodies following treatment with anti-MIF

    Measured: 14 months

  11. Anti-MIF antibody in tumor tissues, bound and/or unbound to active MIF (where applicable)

    Measured: 14 Months

  12. Levels of other potential biomarkers in tumor tissue (where applicable)

    Measured: 14 Months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Jan 2013 (estimated)
  2. Study start14 Jun 2012
  3. Primary completion28 Jul 2016
  4. Study completion28 Jul 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
68 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01765790
Sponsor's protocol ID
391101
Other IDs
2013-002870-31
Status last verified
May 2021
First submitted
9 Jan 2013
Last updated
5 May 2021
Results posted
No
Data monitoring committee
No
Individual data sharing
Yes: Takeda provides access to the de-identified individual participant data (IPD) for eligible studies to aid qualified researchers in addressing legitimate scientific objectives (Takeda's data sharing commitment is available on https://clinicaltrials.takeda.com/takedas-commitment?commitment=5). These IPDs will be provided in a secure research environment following approval of a data sharing request, and under the terms of a data sharing agreement.

Publications

  • Mahalingam D, Patel MR, Sachdev JC, Hart LL, Halama N, Ramanathan RK, Sarantopoulos J, Volkel D, Youssef A, de Jong FA, Tsimberidou AM. Phase I study of imalumab (BAX69), a fully human recombinant antioxidized macrophage migration inhibitory factor antibody in advanced solid tumours. Br J Clin Pharmacol. 2020 Sep;86(9):1836-1848. doi: 10.1111/bcp.14289. Epub 2020 Apr 12.

    PubMed 32207164

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody in people with Metastatic Adenocarcinoma of the Colon or Rectum and Malignant Solid Tumors, run by Baxalta now part of Shire at 5 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 May 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in United States, Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of participants experiencing serious adverse events (SAEs) and/or adverse events (AEs) regardless of causality (time frame: 14 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01765790, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2021; AzTrials last refreshed its copy on 7 Nov 2026.

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