Phase II Clinical Trial of NPC-06 in Patients With Neuropathic Pain in Cancer
NCT ID: NCT03773055
Last Updated: 2020-11-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE2
7 participants
INTERVENTIONAL
2019-04-03
2020-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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NPC-06 (High dosage)
18 mg (iv) in Day 1 as an induction dosage and 9 mg (iv) in Day 2 - 7 as a maintenance dosage
NPC-06
Patients will receive once a day for 7 days.
NPC-06 (Low dosage)
15 mg (iv) in Day 1 as an induction dosage and 6 mg (iv) in Day 2 - 7 as a maintenance dosage
NPC-06
Patients will receive once a day for 7 days.
Placebo
Saline will be administered intravenously
NPC-06
Patients will receive once a day for 7 days.
Interventions
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NPC-06
Patients will receive once a day for 7 days.
Eligibility Criteria
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Inclusion Criteria
2. Both genders
3. Patients who can admit to hospital for all assessment duration from first administration until the next day of final administration. (including the hospitalized patient )
4. Patients who are diagnosed and informed as cancer (including sarcoma, lymphoma and multiple myeloma)
5. Patients who are diagnosed as neuropathic pain by neurological examination and imaging findings
6. Patients who NRS score of average persistent pain is higher than 4, even they were treated with level 3 of WHO three-step analgesic ladder at the observation period.
7. Patients who NRS score at the time of first administration and NRS score of persistent pain in the past 24 hours are higher than 4.
8. Patients who average number of daily rescue medication use during observation period is less than 6.
9. Patients who are predicted to survive longer than 3 month.
10. Patients who ECOG Performance Status (PS) score is 0 to 3.
11. Patients who (or whose legally acceptable representative if the patient is underage) provide a written consent at their own will with a full understanding after receiving a sufficient explanation on participation in the study
Exclusion Criteria
2. Patients who have leukemia as a complication.
3. Patients who have a primary brain neoplasm or a metastatic brain neoplasm as a complication.
4. Patients who have epilepsy, serious psychiatric or neurological disease ( i. e. dementia, Parkinson disease or schizophrenic disorder) or consciousness disturbance as a complication.
5. Patients who have primary trigeminal neuralgia, diabetic neuropathy, post herpetic neuralgia or acute herpes zoster pain as a complication.
6. Patients who has other serious pain which affect the evaluation of neuropathic pain in cancer.
7. Patients who have sinus bradycardia or serious disturbance of conduction system.
8. Patients who have history of hypersensitivity against hydantoin compound.
9. Patients who are administrated tadalafil (for pulmonary hypertension), rilpivirine, asunaprevir, daclatasvir, vaniprevir, macitentan or sofosbuvir.
10. Patients who are administrated methadone.
11. Patients who have complications such as serious heart disease, hepatic function disorder or renal function disorder which severity are considered by investigator as grade 3 or more severe with reference to ''Concerning classification criteria for seriousness of adverse drug reactions of medical agents'' (except cancer).
12. Patients who received surgical treatment or internal radiation therapy in past three month before the first day of pre observation period.
13. Patients who are treated nerve block, radiation therapy, spinal cord stimulation or surgical treatment for the part of neuropathic pain in past one month before the first day of pre observation period.
14. Patients who change the usage or dosage of medication for cancer as primal disease in the past two week before the first day of the pre observation period, or patients who are predicted not to continue the treatment without change in the medication while this clinical trial.
15. Patients who are administrating with fosphenytoin, phenytoin or ethotoin or have taken these drugs as medication for neuropathic pain.
16. Patients who have participated in other clinical trial and have taken a trial drug in past three month before the first day of pre observation period.
17. Female patients who are pregnant or lactating or who may be pregnancy in the period of the clinical trial.
18. Patients who can not agree to prevent contraception appropriately following the direction of the Investigator or the sub-investigator.
19. Any other patients who are considered by the investigator as unsuitable for participation in the trial.
16 Years
ALL
No
Sponsors
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Nobelpharma
INDUSTRY
Responsible Party
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Locations
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Keio Hospital
Shinjuku-Ku, Tokyo, Japan
Countries
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Other Identifiers
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NPC-06-4
Identifier Type: -
Identifier Source: org_study_id