Preventive Treatment of Oxaliplatin Induced Peripheral Neuropathy in Metastatic Colorectal Cancer (POLAR-M)



Status:Recruiting
Conditions:Colorectal Cancer, Cancer, Neurology
Therapuetic Areas:Neurology, Oncology
Healthy:No
Age Range:18 - Any
Updated:2/9/2019
Start Date:October 1, 2018
End Date:September 2022
Contact:Stefan Carlsson, MD
Email:stefan.carlsson@pledpharma.se
Phone:+46709641009

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A Phase 3, Double-blind, Multicenter, Placebo-controlled Study of PledOx Used on Top of Modified FOLFOX6 (5-FU/FA and Oxaliplatin) to Prevent Chemotherapy Induced Peripheral Neuropathy (CIPN) in Patients With First-line mCRC

This study evaluates the investigational drug PledOx in the prevention of chronic
chemotherapy induced peripheral neuropathy (CIPN) induced by the drug oxaliplatin.

Oxaliplatin, in combination with 5-fluorouracil plus folinate (or capecitabine), has
increased survival in stage III colorectal cancer and prolonged life in stage IV patients,
but its use is compromised because of severe toxicity. Chemotherapy-induced peripheral
neuropathy (CIPN) is the most problematic dose-limiting toxicity of oxaliplatin. No
treatments have been clinically proven to prevent CIPN. There is a body of evidence that CIPN
is caused by cellular oxidative stress. Clinical and preclinical data suggest that the
manganese chelate and superoxide dismutase mimetic mangafodipir (MnDPDP) and calmangafodipir
(Ca4Mn(DPDP)5) are efficacious inhibitors of CIPN and other conditions caused by cellular
oxidative stress, without interfering negatively with the tumoricidal activity of
chemotherapy.

Inclusion Criteria:

- Signed informed consent form before any study related assessments and willing to
follow all study procedures.

- Male or female aged >=18 years.

- Metastatic (stage IV) CRC, pathologically confirmed adenocarcinoma of the colon or
rectum.

- No prior chemotherapy (within the previous 12 months) and/or biologic/targeted therapy
for mCRC.

- Measurable disease according to RECIST 1.1.

- Patient indicated for at least 3 months of oxaliplatin-based chemotherapy (without any
pre-planned treatment breaks) and without any clinically observed neurological
disorders.

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

- Adequate hematological parameters: hemoglobin >=100 g/L, absolute neutrophil count
(ANC) >=1.5 x 10^9 /L, platelets >=100 x 10^9 /L.

- Adequate renal function: creatinine clearance >50 cc/min using the Cockroft and Gault
formula or measured.

- Adequate hepatic function: total bilirubin <=1.5 times the upper limit of normal (ULN)
(except in the case of known Gilbert's syndrome); aspartate aminotransferase (AST) and
alanine aminotransferase (ALT) <=3 times ULN (AST and ALT <=5 times ULN in case of
liver metastases).

- Baseline blood manganese (Mn) level <2.0 times ULN.

- For patients with a history of diabetes mellitus, HbA1c <=7%.

- Negative pregnancy test for females of child-bearing potential.

- For men and females of childbearing potential, use of adequate contraception (oral
contraceptives, intrauterine device or barrier method of contraception in conjunction
with spermicidal jelly or surgically sterile) while on study drug and for at least 6
months after completion of study therapy.

Exclusion Criteria:

- Any unresolved toxicity by Common Terminology Criteria for Adverse Events Version
(CTCAE v4.03) > Grade 1 from previous anti-cancer therapy (including radiotherapy),
except alopecia.

- Any grade of neuropathy from any cause.

- Any prior oxaliplatin-based chemotherapy <1 year before the randomization.

- Any evidence of severe or uncontrolled systemic diseases (e.g., unstable or
uncompensated respiratory, cardiac, unresolved bowel obstruction, hepatic or renal
disease).

- Chronic infection or uncontrolled serious illness causing immunodeficiency.

- A surgical incision that is not healed.

- Significant hemorrhage (>30 mL/bleeding episode in previous 3 months), hemoptysis (>5
mL fresh blood in previous 4 weeks) or thrombotic event (including transient ischemic
attack) in the previous 12 months if the patient is expected to receive
anti-VEGF/VEGFR therapy.

- Known hypersensitivity to any of the components of mFOLFOX6 and, if applicable,
biological therapies to be used in conjunction with the chemotherapy regimen or any of
the excipients of these products.

- History of other malignancies (except for adequately treated basal or squamous cell
carcinoma or carcinoma in situ) within 5 years, unless the patient has been disease
free for that other malignancy for at least 2 years.

- Known dihydropyrimidine dehydrogenase deficiency.

- Pre-existing neurodegenerative disease (e.g., Parkinson's, Alzheimer's, Huntington's)
or neuromuscular disorder (e.g., multiple sclerosis, amyotrophic lateral sclerosis,
polio, hereditary neuromuscular disease).

- Major psychiatric disorder (major depression, psychosis), alcohol and/or drug abuse.

- Patients with a history of second or third degree atrioventricular block or a family
heredity.

- A history of a genetic or familial neuropathy.

- Treatment with any investigational drug within 30 days prior to randomization.

- Pregnancy, lactation or reluctance to using contraception.

- Any other condition that, in the opinion of the Investigator, places the patient at
undue risk.

- Previous exposure to mangafodipir or calmangafodipir.

- Welders, mine workers or other workers in occupations (current or past) where high
manganese exposure is likely.
We found this trial at
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Canton, Ohio 44708
Phone: 330-489-1274
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701 Doctors Dr
Kinston, North Carolina 28504
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Kinston Medical Specialists offers comprehensive medical services for all ages. Whether it’s a case of...
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Ames, Iowa 50010
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Bethesda, Maryland 20817
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Billings, New York 59102
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Bismarck, North Dakota 58501
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Bronx, New York 10461
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Charleston, South Carolina 29403
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Dublin, Georgia 31021
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Flemington, New Jersey 08822
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Fresno, California 93720
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Grand Island, Nebraska 68803
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Greenbrae, California 94904
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30 Prospect Ave
Hackensack, New Jersey 07601
(201) 996-2000
Phone: 201-966-5900
Hackensack University Medical Center Hackensack University Medical Center, part of the Hackensack University Health Network,...
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Higashi-ku, Fukuoka 81285
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La Crosse, Wisconsin 54601
Phone: 608-785-0940
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450 Lakeville Rd
Lake Success, New York 11040
(516) 734-8900
Phone: 631-638-0846
Monter Cancer Center The Monter Cancer Center is a unique facility dedicated to providing state-of-the-art...
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Miami Beach, Florida 33140
Phone: 305-674-2625
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Minot, North Dakota 58701
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254 Easton Ave
New Brunswick, New Jersey 08901
(732) 745-8600
Phone: 732-246-4882
Saint Peter's University Hospital Located in New Brunswick, NJ, Saint Peter's University Hospital has been...
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2776 Enterprise Rd # 100
Orange City, Florida 32763
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Pismo Beach, California 93449
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Saint Louis, Missouri 63141
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Santa Rosa, California 95403
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Seattle, Washington 98101
(888) 862-2737
Phone: 206-223-6600
Virginia Mason Medical Center Established in 1920, Virginia Mason began as an 80-bed hospital with...
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1309 W 17th Street
Sioux Falls, South Dakota 57104
(605) 328-8000
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Springfield, Missouri 65804
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Temple, Texas 76504
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818 N. Emporia, #403
Wichita, Kansas 67214
(316) 262-4467
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Cancer Center of Kansas The physicians of Cancer Center are hematologists and oncologists. The staff...
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