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.
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
- Conditions the study is for
- Metastatic Adenocarcinoma of the Colon or Rectum, Malignant Solid Tumors
- 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
Germany1 site
Nationales Centrum für Tumorerkrankungen (NCT) Heidelberg
Heidelberg, 69120
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 group | Role | What they receive |
|---|---|---|
| Malignant Solid Tumor (Arm 1) | Experimental | Dose 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) | Experimental | Dose 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.
Number of participants experiencing serious adverse events (SAEs) and/or adverse events (AEs) regardless of causality
Measured: 14 months
Secondary outcomes (12)
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
Tumor response
Measured: 14 months
Levels of free active MIF and free total MIF in plasma and tumor tissue (where applicable)
Measured: 14 months
Change in levels of tumor-associated biomarkers, if applicable based on cancer type, following treatment with anti-MIF antibody
Measured: 14 months
Number of serious adverse events (SAEs) and/or adverse events (AEs), regardless of causality
Measured: 14 Months
Number of participants experiencing related serious adverse events (SAEs) and/or adverse events (AEs)
Measured: 14 months
Number of related serious adverse events (SAEs) and/or adverse events (AEs)
Measured: 14 months
Number of dose limiting toxicities (DLTs)
Measured: 14 months
Number of participants experiencing dose limiting toxicity (DLT)
Measured: 14 months
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
Anti-MIF antibody in tumor tissues, bound and/or unbound to active MIF (where applicable)
Measured: 14 Months
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.
- First posted10 Jan 2013 (estimated)
- Study start14 Jun 2012
- Primary completion28 Jul 2016
- Study completion28 Jul 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Metastatic Adenocarcinoma of the Colon or RectumStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Baxalta now part of Shire
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Study Director, Study director, Takeda
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
Study at a glance
From the registry record, last updated by the sponsor on 5 May 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT01765790
- Acronym / sponsor ID
- 391101
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 68 participants (actual)
- Lead sponsor
- Baxalta now part of ShireIndustry (pharma, biotech, devices)
- Study start
- 14 Jun 2012 (actual)
- Primary completion
- 28 Jul 2016 (actual)
- Study completion
- 28 Jul 2016 (actual)
- First posted
- 10 Jan 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Malignant Solid Tumor (Arm 1) | Experimental | Biological: Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) AntibodyDose 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). |
| Metastatic Adenocarcinoma of the Colon or Rectum (Arm 2) | Experimental | Biological: Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) AntibodyDose 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). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody* Dosing every 2 weeks * Intravenous injection | Biological | Malignant Solid Tumor (Arm 1) |
| Anti-Macrophage Migration Inhibitory Factor (Anti-MIF) Antibody* Dosing weekly * Intravenous injection | Biological | Metastatic Adenocarcinoma of the Colon or Rectum (Arm 2) |
Primary outcome
Number of participants experiencing serious adverse events (SAEs) and/or adverse events (AEs) regardless of causality
Time frame: 14 months
12 secondary outcomes
Plasma pharmacokinetic parameters
Time frame: 28 days
Tumor response
Time frame: 14 months
Levels of free active MIF and free total MIF in plasma and tumor tissue (where applicable)
Time frame: 14 months
Change in levels of tumor-associated biomarkers, if applicable based on cancer type, following treatment with anti-MIF antibody
Time frame: 14 months
Number of serious adverse events (SAEs) and/or adverse events (AEs), regardless of causality
Time frame: 14 Months
Number of participants experiencing related serious adverse events (SAEs) and/or adverse events (AEs)
Time frame: 14 months
Number of related serious adverse events (SAEs) and/or adverse events (AEs)
Time frame: 14 months
Number of dose limiting toxicities (DLTs)
Time frame: 14 months
Number of participants experiencing dose limiting toxicity (DLT)
Time frame: 14 months
Number of participants who develop binding and/or neutralizing anti-anti-macrophage migration inhibitory factor (anti-MIF) antibodies following treatment with anti-MIF
Time frame: 14 months
Anti-MIF antibody in tumor tissues, bound and/or unbound to active MIF (where applicable)
Time frame: 14 Months
Levels of other potential biomarkers in tumor tissue (where applicable)
Time frame: 14 Months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 May 2021.
- Derived from this study: PubMed 32207164Mahalingam 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.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Study Director study director
Takeda
5 sites in 2 countries: see every site and its status.
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.