Tivantinib in Treating Patients With Relapsed, or Relapsed and Refractory Multiple Myeloma

• Sponsor: National Cancer Institute (NCI) (NIH)
• Overall Status: Completed
• CT.gov ID: NCT01447914
• Collaborator: (none)
• Enrollment: 16
• Location: 1
• Arm: 1
• Duration (Months): 29
• Patients Per Site Per Month: 0.6

Study Details

Study Description

Brief Summary

This phase II trial studies the side effects and how well tivantinib works in treating patients with relapsed, or relapsed and refractory multiple myeloma. Tivantinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

Condition or Disease	Intervention/Treatment	Phase
Refractory Multiple Myeloma	Drug: Tivantinib; Other: Diagnostic laboratory biomarker analysis; Other: Questionnaire administration; Procedure: Quality-of-life assessment	Phase 2

Detailed Description

PRIMARY OBJECTIVES:

1. To determine the overall response rate of patients with relapsed, or relapsed and refractory multiple myeloma treated with the c-Met inhibitor ARQ 197 (tivantinib) as a single agent.

2. To define the toxicities of single agent ARQ 197 in a population of patients with relapsed, or relapsed and refractory multiple myeloma.

SECONDARY OBJECTIVES:

1. To obtain preliminary evidence of the durability of responses to single agent ARQ 197, including the progression free survival (PFS), the duration of response (DOR), and the time to next treatment (TTNT).

2. To correlate the activation status of the hepatocyte growth factor (HGF)/c-Met pathway in primary myeloma cells at baseline, as defined by gene expression profiling and reverse phase protein array data, with the above measures of efficacy of ARQ 197.

3. To correlate serum and marrow HGF, HGF activator (HGFA), and soluble c-Met (sc-Met) levels with the activation status of the HGF/c-Met pathway in primary myeloma cells at baseline, and with the above measures of efficacy of ARQ 197.

TERTIARY OBJECTIVES:

1. To evaluate the symptom burden of relapsed, or relapsed and refractory multiple myeloma patients undergoing therapy with single agent ARQ 197 using the M. D. Anderson Symptom Inventory (MDASI) and its multiple myeloma module (MDASI-MM) II. To evaluate the impact of therapy with single agent ARQ 197 for relapsed, or relapsed and refractory multiple myeloma on patient reported outcomes using the European Organization for Research on the Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) Core 30 (QLQ-C30), and the myeloma-specific module QLQ-MY20.

2. To evaluate the impact of therapy with single agent ARQ 197 for relapsed, or relapsed and refractory multiple myeloma on the ability to collect stem cells in any patients who go on to undergo subsequent stem cell mobilization.

OUTLINE:

Patients receive tivantinib orally (PO) twice daily (BID) on days 1-28. Courses continue every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo blood, urine, and bone marrow collection for gene expression profile, proteomic profiling, and other correlative studies. Patients may complete the MDASI and its MDASI-MM, the EORTC QLQ-C30, and the myeloma-specific module QLQMY20 questionnaires at baseline and periodically during study.

After completion of study treatment, patients are followed up for 30 days.

Study Design

• Study Type: Interventional
• Actual Enrollment: 16 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase II Study of the c-Met Inhibitor ARQ 197 in Patients With Relapsed, or Relapsed and Refractory Multiple Myeloma
• Study Start Date: Nov 1, 2011
• Actual Primary Completion Date: Mar 1, 2014
• Actual Study Completion Date: Apr 1, 2014

Arms and Interventions

Arm

Intervention/Treatment

Experimental: ARQ 197 Treatment (Tivantinib) Oral Tivantinib 360 mg twice daily continuously for each day (days 1-28) of every 4-week treatment cycle (taken as three tablets of 120 mg each). Courses continue every 28 days in the absence of disease progression or unacceptable toxicity.

Drug: Tivantinib; Given at a dose of 360 mg oral (PO) twice daily continuously for each day of every 4-week treatment cycle, which will be taken as three tablets of 120 mg each.; Other Names: ARQ 197 c-Met Inhibitor ARQ 197 ; Other: Diagnostic laboratory biomarker analysis; Correlative studies; Other: Questionnaire administration; Ancillary studies; Procedure: Quality-of-life assessment; Ancillary studies; Other Names: quality of life assessment

Outcome Measures

Primary Outcome Measures

1. Overall Response Rate (ORR) [Up to 30 days]

   ORR using International Myeloma Working Group Response Criteria, achieve at least a partial response (PR) or better: Stringent Complete Response (sCR), Complete Response (CR), Very Good Partial Response (VGPR) or Partial Response (PR): CR: Negative immunofixation on serum and urine and disappearance of any soft tissue plasmacytomas and <5% plasma cells in bone marrow; sCR: CR+Normal free light chain ratio and absence of clonal cells in bone marrow by immunohistochemistry or immunofluorescence; PR: ≥50% reduction of serum M-protein and reduction in 24-hour urinary M-protein by ≥90%; VGPR: Serum and urine M-protein detectable by immunofixation but not on electrophoresis or 90% or greater reduction in serum M-protein plus urine M-protein level <100mg per 24 hour; Stable Disease (SD): Not CR, VGPR, PR or progressive disease; Progressive Disease (PD):>25% from lowest value Serum and/or Urine M-component, new lesions or soft tissue plasmacytomas, or hypercalcemia.

2. Toxicities of Single Agent Tivantinib: Grade 3 Nonhematologic or Grade 4 Hematologic Toxicities According to the Common Terminology Criteria for Adverse Events (CTCAE), Version 4 [Up to 30 days]

   Toxicities with a grade 3 nonhematologic or grade 4 hematologic toxicities according to CTCAE, version 4. Grade 3 and estimated with a 95% credible interval. Summary statistics will be provided for continuous variables.

Secondary Outcome Measures

1. Time to Next Treatment (TTNT) [From registration on trial to next treatment or death due to any cause, whichever comes first]

   Kaplan and Meier product limit methods will be used to estimate the TTNT with 95% confidence intervals.

Other Outcome Measures

1. Duration of Response [From first observation of partial response to the time of disease progression, assessed up to 30 days]

   Kaplan and Meier product limit methods will be used to estimate the DOR with 95% confidence intervals.

2. Progression-free Survival (PFS) [From start of the treatment to disease progression or death (regardless of cause of death), whichever comes first, assessed up to 30 days]

   Kaplan and Meier product limit methods will be used to estimate the median PFS with 95% confidence intervals. Furthermore, the univariate and multivariate Cox proportional hazards regression model will be used to identify prognostic factors for PFS.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Patients must have been previously diagnosed with histologically or cytologically confirmed symptomatic multiple myeloma, which requires the presence of all three of the following International Myeloma Working Group criteria, except as noted:

• Clonal bone marrow plasma cells >= 10%

• A monoclonal protein in either serum or urine

• Evidence of end-organ damage that can be attributed to the underlying plasma cell proliferative disorder (to include one of the following):

• Hypercalcemia (corrected calcium > 2.75 mmol/L or 11.5 mg/dL)

• Renal insufficiency attributable to myeloma (serum creatinine > 1.9 mg/dL)

• Anemia; normochromic, normocytic with a hemoglobin value >= 2 g/dL below the lower limit of normal, or a hemoglobin or < 10 g/dL

• Bone lytic lesions, severe osteopenia, or pathologic fractures

• Patients with a biopsy-proven plasmacytoma and either a serum or urine monoclonal protein will also be considered to have met the diagnostic criteria for multiple myeloma in the absence of clonal marrow plasmacytosis of >= 10%

• Patients must have measurable disease, as defined by at least one of the following:

• Serum monoclonal protein level >= 0.5 g/dL for immunoglobulin (Ig)G, IgA, or IgM disease

• Monoclonal protein or total serum IgD >= 0.5 g/dL for IgD disease

• Urinary M-protein excretion of >= 200 mg over a 24-hour period

• Involved free light chain level >= 10 mg/dL, along with an abnormal free light chain ratio

• Patients must have had at least one, but not more than four prior lines of therapy for their disease, with lines of therapy being separated by the presence of documented disease progression; using this definition, treatment with induction therapy, followed by high-dose chemotherapy and autologous stem cell transplantation, and finally by maintenance therapy, would constitute one line, provided that multiple myeloma did not meet criteria for progression at any time during this period

• Patients with relapsed disease will be considered to be those who have had progression, as defined above, off of any therapy, and who completed their therapy more than 60 days prior to the finding of progression; patients with relapsed and refractory disease will be considered to be those who have had progression, as defined above, while still on their last line of therapy, or who progressed within 60 days of finishing their most recent therapy

• Patients must have completed their most recent drug therapy directed at multiple myeloma in the following time frames:

• Chemotherapy, biological therapy, immunotherapy, or an investigational therapy at least 3 weeks prior to starting c-Met inhibitor ARQ197

• Corticosteroids at least 3 weeks prior to starting ARQ 197, except for a dose equivalent to dexamethasone of no greater than 4 mg/day

• Nitrosoureas, nitrogen mustards, mitomycin C, or monoclonal antibodies at least 6 weeks prior to starting ARQ 197

• Autologous stem cell transplantation at least 12 weeks prior to starting ARQ 197

• Allogeneic stem cell transplantation at least 24 weeks prior to starting ARQ 197, and these patients must also not have moderate to severe active acute or chronic graft-versus-host disease

• Patients must be willing and able to provide voluntary written informed consent, with the understanding that consent may be withdrawn by the subject at any time without prejudice to their future medical care

• Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 (Karnofsky

= 60%)

• Absolute neutrophil count (ANC) >= 1,000 cells/mm^3 without growth factors within 1 week of the initiation of treatment

• Total white blood cell count (WBC) >= 2,000 cells/mm^3 without growth factors within 1 week of the initiation of treatment

• Hemoglobin >= 8 g/dL without red blood cell transfusions within 2 weeks of the initiation of treatment

• Platelet counts of >= 100,000 cells/mm^{3 for patients who have bone marrow plasmacytosis of < 50%, or >= 50,000 cells/mm}3 for patients who have bone marrow plasmacytosis of >= 50%

• Total bilirubin =< 1.5 times the upper limit of the institutional normal (ULN) values

• Total aspartate aminotransferase (AST) (serum glutamic oxaloacetic acid transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 times ULN values

• Serum creatinine within the institutional normal limits OR if the creatinine is elevated, creatinine clearance (CrCl) >= 30 mL/min., as measured by a 24-hour urine collection, or estimated by the Cockcroft and Gault formula

• Patients must have evidence of adequate cardiac function, as defined by the following:

• Absence of New York Heart Association (NYHA) class II, III, or IV congestive heart failure

• Absence of uncontrolled angina or hypertension

• Absence of myocardial infarction in the previous 6 months

• Absence of clinically significant bradycardia or other uncontrolled cardiac arrhythmia defined as grade 3 or 4 according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 4.0

• Patients who have received radiation therapy must have completed this at least 4 weeks prior to starting therapy with ARQ 197, with the following exceptions:

• Local radiation therapy to enhance bone healing of a pathologic fracture may have been performed, as long as it was completed at least 2 weeks prior to starting ARQ 197

• Local radiation therapy to treat post-fracture pain that is refractory to analgesics may have been performed, as long as it was completed at least 2 weeks prior to starting ARQ197

• Patients who have undergone any recent major surgery must have done so at least 4 weeks prior to starting therapy with ARQ 197, with the following exceptions:

• Vertebroplasty and/or kyphoplasty, which must have been performed at least 1 week prior to starting ARQ 197

• Planned elective surgery unrelated to the patient's diagnosis of multiple myeloma, such as hernia repair, may be allowed, at the discretion of the Principal Investigator, as long as it was performed at least 2 weeks prior to starting ARQ 197, and patients have recovered fully from this procedure

• Human immunodeficiency virus (HIV)-seropositive patients with acceptable organ function who meet the patient selection criteria, and who are not on combination antiretroviral therapy, and whose absolute CD4+ count is >= 400 cells per cubic millimeter of blood, will be eligible; however, HIV positive patients on combination antiretroviral therapy will be ineligible

• Male patients must agree to use an adequate method of contraception for the duration of the study since the effects of ARQ 197 on the developing human fetus are unknown; female patients must be either post- menopausal, free from menses for >= 2 years, surgically sterilized, or willing to use two adequate barrier methods of contraception to prevent pregnancy, or must agree to abstain from heterosexual activity throughout the study; female patients of childbearing potential must have a negative serum (beta-human chorionic gonadotropin [beta-HCG]) or urine pregnancy test before receiving the first dose of ARQ 197; should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately

Exclusion Criteria:

• Patients who are receiving any concurrent investigational agent with known or suspected activity against multiple myeloma, or those whose adverse events due to agents administered more than 4 weeks earlier have not recovered to a severity of grade 0 or grade 1

• Patients who have known central nervous system involvement with multiple myeloma will be excluded from this clinical trial

• Patients who have previously been treated with another agent targeting the HGF/c-Met axis, including either monoclonal antibodies to HGF or c-Met, or small molecule inhibitors of c-Met

• Patients with a known history of allergic reactions attributed to compounds of similar chemical or biologic composition to ARQ 197

• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements, in the opinion of the Principal Investigator

• Pregnant or lactating women are excluded from this study

• HIV positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with ARQ 197; however, HIV seropositive patients with acceptable organ function who meet the patient selection criteria, and who are not on combination antiretroviral therapy, will be eligible

• Patients with non-secretory multiple myeloma, active plasma cell leukemia, defined as either having 20% of peripheral white blood cells comprised of CD138+ plasma cells, or an absolute plasma cell count of 2 x 10^9/L, known amyloidosis, or known POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes)

• Patients who have required plasmapheresis and exchange less than 2 weeks prior to initiation of therapy with ARQ 197

• Patients with known active hepatitis A, B, and/or C infection

• Patients with a "currently active" second malignancy, other than non-melanoma skin cancer and carcinoma in situ of the cervix, should not be enrolled; patients are not considered to have a "currently active" malignancy if they have completed therapy for a prior malignancy, are disease free from prior malignancies for > 5 years, and are considered by their physician to be at less than 30% risk of relapse; in addition, patients with basal cell carcinoma of the skin, superficial carcinoma of the bladder, carcinoma of the prostate with a current prostate-specific antigen (PSA) value of < 0.5 ng/mL, or cervical intraepithelial neoplasia will be eligible; finally, patients who are on hormonal therapy for a history of either prostate cancer or breast cancer may enroll, provided that there has been no evidence of disease progression during the previous three years

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	M D Anderson Cancer Center	Houston	Texas	United States	77030

Sponsors and Collaborators

• National Cancer Institute (NCI)

Investigators

• Principal Investigator: Robert Orlowski, M.D. Anderson Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• University of Texas MD Anderson Cancer Center Official Website

Publications

None provided.

• Responsible Party: National Cancer Institute (NCI)
• ClinicalTrials.gov Identifier: NCT01447914
• Other Study ID Numbers: NCI-2011-03470; NCI-2011-03470; CDR0000712984; 2011-0197; 8984; U01CA062461; P30CA016672; N01CM00039
• First Posted: Oct 6, 2011
• Last Update Posted: Aug 28, 2019
• Last Verified: Aug 1, 2019

• Keywords provided by National Cancer Institute (NCI): c-Met Inhibitor ARQ-197; tivantinib; multiple myeloma; plasma cell proliferative disorder; Hypercalcemia; hematologic malignancy; plasma cell dyscrasia; cast nephropathy; amyloidosis; osteolysis; Renal insufficiency; Anemia; Bone lytic lesions; severe osteopenia; pathologic fractures; biopsy-proven plasmacytoma
• Additional relevant MeSH terms: Multiple Myeloma; Neoplasms, Plasma Cell

Study Results

Participant Flow

Recruitment Details	Total Recruitment Period: November 30, 2011 to August 1, 2013. All recruitment done at University of Texas (UT) MD Anderson Cancer Center.

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Period Title: Overall Study
STARTED	16
COMPLETED	16
NOT COMPLETED	0

Baseline Characteristics

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Overall Participants	16
Age (years) [Mean (Full Range) ]
Mean (Full Range) [years]	66.3
Sex: Female, Male (Count of Participants)
Female	7 43.8%
Male	9 56.3%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino	3 18.8%
Not Hispanic or Latino	13 81.3%
Unknown or Not Reported	0 0%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native	0 0%
Asian	1 6.3%
Native Hawaiian or Other Pacific Islander	0 0%
Black or African American	2 12.5%
White	13 81.3%
More than one race	0 0%
Unknown or Not Reported	0 0%
Region of Enrollment (participants) [Number]
United States	16 100%
Prior Stem Cell Transplantation (SCT) (participants) [Number]
Prior SCT	10 62.5%
No Prior SCT	6 37.5%

Outcome Measures

1. Primary Outcome

Title	Overall Response Rate (ORR)
Description	ORR using International Myeloma Working Group Response Criteria, achieve at least a partial response (PR) or better: Stringent Complete Response (sCR), Complete Response (CR), Very Good Partial Response (VGPR) or Partial Response (PR): CR: Negative immunofixation on serum and urine and disappearance of any soft tissue plasmacytomas and <5% plasma cells in bone marrow; sCR: CR+Normal free light chain ratio and absence of clonal cells in bone marrow by immunohistochemistry or immunofluorescence; PR: ≥50% reduction of serum M-protein and reduction in 24-hour urinary M-protein by ≥90%; VGPR: Serum and urine M-protein detectable by immunofixation but not on electrophoresis or 90% or greater reduction in serum M-protein plus urine M-protein level <100mg per 24 hour; Stable Disease (SD): Not CR, VGPR, PR or progressive disease; Progressive Disease (PD):>25% from lowest value Serum and/or Urine M-component, new lesions or soft tissue plasmacytomas, or hypercalcemia.
Time Frame	Up to 30 days

Outcome Measure Data

Analysis Population Description

Proportion of participants reported on an intent-to-treat basis.

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	16
Stable Disease	4 25%
Progressive Disease	7 43.8%
Not Evaluable	5 31.3%

2. Primary Outcome

Title	Toxicities of Single Agent Tivantinib: Grade 3 Nonhematologic or Grade 4 Hematologic Toxicities According to the Common Terminology Criteria for Adverse Events (CTCAE), Version 4
Description	Toxicities with a grade 3 nonhematologic or grade 4 hematologic toxicities according to CTCAE, version 4. Grade 3 and estimated with a 95% credible interval. Summary statistics will be provided for continuous variables.
Time Frame	Up to 30 days

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	16
Non-Hematological Grade 3- Hypertension	1 6.3%
Non Hematological Grade 3- Syncope	2 12.5%
Non Hematological Grade 3- Pulmonari emboli	1 6.3%
Hematological Grade 3- Neutropenia	4 25%
Non Hematological Grade 3- Fatigue	1 6.3%
Non Hematological Grade 3- Cough	1 6.3%
Non Hematological Grade 3- Bacteremia	1 6.3%
Non Hematological Grade 3- Anorectal Infection	1 6.3%
Non Hematological Grade 3- Rectal Pain	1 6.3%
Non Hematological Grade 3- Rib Pain	1 6.3%

3. Secondary Outcome

Title	Time to Next Treatment (TTNT)
Description	Kaplan and Meier product limit methods will be used to estimate the TTNT with 95% confidence intervals.
Time Frame	From registration on trial to next treatment or death due to any cause, whichever comes first

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	16
Median (95% Confidence Interval) [number of months]	4

4. Other Pre-specified Outcome

Title	Duration of Response
Description	Kaplan and Meier product limit methods will be used to estimate the DOR with 95% confidence intervals.
Time Frame	From first observation of partial response to the time of disease progression, assessed up to 30 days

Outcome Measure Data

Analysis Population Description

No participants responded to the therapy and no analyses were done

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	0

5. Other Pre-specified Outcome

Title	Progression-free Survival (PFS)
Description	Kaplan and Meier product limit methods will be used to estimate the median PFS with 95% confidence intervals. Furthermore, the univariate and multivariate Cox proportional hazards regression model will be used to identify prognostic factors for PFS.
Time Frame	From start of the treatment to disease progression or death (regardless of cause of death), whichever comes first, assessed up to 30 days

Outcome Measure Data

Analysis Population Description

No participants responded to the therapy and no analyses was done.

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	0

6. Post-Hoc Outcome

Title	Cycles of Tivantinib Treatment Administered
Description	Number of treatment cycles completed by study participants.
Time Frame	From start of participant treatment to completion or disease progression; assessed up to 16 months

Outcome Measure Data

Analysis Population Description

No participants responded to the therapy and no analyses were done

Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
Measure Participants	16
Mean (Full Range) [number of treatment cycles]	4

Adverse Events

Time Frame	Adverse events collected till 30 days of the last dose of the investigational agent and include all who receive any amount of study drug. Overall collection period January 2012 to February 2014.
Arm/Group Title	Tivantinib Treatment
Arm/Group Description	Oral Tivantinib 360 mg twice daily continuously for each day of every 28 day treatment cycle (taken as three tablets of 120 mg each)
All Cause Mortality
	Tivantinib Treatment
	Affected / at Risk (%)	# Events
Total	/ (NaN)
Serious Adverse Events
	Tivantinib Treatment
	Affected / at Risk (%)	# Events
Total	8/16 (50%)
Blood and lymphatic system disorders
Neutropenia (Neutrophil count decreased)	5/16 (31.3%)	9
Cardiac disorders
Hypertension	1/16 (6.3%)	1
Syncope	2/16 (12.5%)	2
General disorders
Fatigue	1/16 (6.3%)	1
Pain	2/16 (12.5%)	2
Infections and infestations
Bacteremia Infection	1/16 (6.3%)	1
Anorectal Infection	1/16 (6.3%)	1
Respiratory, thoracic and mediastinal disorders
Cough	1/16 (6.3%)	1
Multiple pulmonary emboli	1/16 (6.3%)	1
Other (Not Including Serious) Adverse Events
	Tivantinib Treatment
	Affected / at Risk (%)	# Events
Total	16/16 (100%)
Blood and lymphatic system disorders
Anemia	3/16 (18.8%)	3
Neutrophil count decreased	5/16 (31.3%)	6
Platelet count decreased	2/16 (12.5%)	2
Cardiac disorders
Hypertension	3/16 (18.8%)	3
Hyperlipidemia	1/16 (6.3%)	1
Sinus bradycardia	3/16 (18.8%)	3
Ear and labyrinth disorders
Tinnitus	1/16 (6.3%)	1
Endocrine disorders
Hypothyroidism	1/16 (6.3%)	1
Diabetes	1/16 (6.3%)	1
Eye disorders
Blurred vision	2/16 (12.5%)	5
Dry eye	3/16 (18.8%)	4
Watering eyes	2/16 (12.5%)	2
Gastrointestinal disorders
Constipation	3/16 (18.8%)	5
Diarrhea	6/16 (37.5%)	7
Diverticulitis flare	1/16 (6.3%)	1
Nausea	2/16 (12.5%)	2
General disorders
Chills	1/16 (6.3%)	1
Fatigue	10/16 (62.5%)	14
Insomnia	2/16 (12.5%)	2
Pain	7/16 (43.8%)	12
Immune system disorders
Allergic rhinitis	2/16 (12.5%)	2
Infections and infestations
Fever	2/16 (12.5%)	2
Flu like symptoms	1/16 (6.3%)	1
Metabolism and nutrition disorders
Creatinine increased	1/16 (6.3%)	1
Hypokalemia	1/16 (6.3%)	1
Musculoskeletal and connective tissue disorders
Edema limbs	2/16 (12.5%)	3
Gait distrubance	1/16 (6.3%)	1
Muscle Discomfort	3/16 (18.8%)	3
Myalgia	6/16 (37.5%)	9
Nervous system disorders
Anxiety	2/16 (12.5%)	2
Depression	1/16 (6.3%)	1
Dizziness	6/16 (37.5%)	8
Headache	2/16 (12.5%)	2
Memory impairment	5/16 (31.3%)	5
Paresthesia	1/16 (6.3%)	1
Peripheral motor neuropathy	10/16 (62.5%)	11
Renal and urinary disorders
Nocturia	6/16 (37.5%)	6
Urinary tract pain	1/16 (6.3%)	1
Respiratory, thoracic and mediastinal disorders
Cough	5/16 (31.3%)	6
Dyspnea	6/16 (37.5%)	9
Rhinorrhea	4/16 (25%)	4
Sinusitis	1/16 (6.3%)	1
Upper Respiratory Infection	4/16 (25%)	4
Wheezing	1/16 (6.3%)	1
Congestion	1/16 (6.3%)	1
Sore Throat	1/16 (6.3%)	1
Postnasal Drip	1/16 (6.3%)	1
Skin and subcutaneous tissue disorders
Alopecia	2/16 (12.5%)	2
Hyperhidrosis	1/16 (6.3%)	1
Rash acneiform	1/16 (6.3%)	3
Skin and subcutaneous tissue disorders	2/16 (12.5%)	2
Rash maculo-papular	1/16 (6.3%)	2

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

Principal Investigators are NOT employed by the organization sponsoring the study.

The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.