Unique ID issued by UMIN | UMIN000007062 |
---|---|
Receipt number | R000007316 |
Scientific Title | A Phase I, Dose-Escalating Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Intrathecal Infusion of KP-100IT through SM-1500 in Subjects with Amyotrophic Lateral Sclerosis (ALS) |
Date of disclosure of the study information | 2012/01/16 |
Last modified on | 2015/07/14 16:41:55 |
A Phase I, Dose-Escalating Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Intrathecal Infusion of KP-100IT through SM-1500 in Subjects with Amyotrophic Lateral Sclerosis (ALS)
A Phase I, Dose-Escalating Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Intrathecal Infusion of KP-100IT through SM-1500 in Subjects with Amyotrophic Lateral Sclerosis (ALS)
A Phase I, Dose-Escalating Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Intrathecal Infusion of KP-100IT through SM-1500 in Subjects with Amyotrophic Lateral Sclerosis (ALS)
A Phase I, Dose-Escalating Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Intrathecal Infusion of KP-100IT through SM-1500 in Subjects with Amyotrophic Lateral Sclerosis (ALS)
Japan |
Amyotrophic lateral sclerosis (ALS)
Neurology |
Others
NO
To evaluate the safety and tolerability of single and multiple intrathecal doses of KP-100IT by assessing adverse events in subjects with ALS
Pharmacokinetics
Phase I
Safety and tolerability of KP-100IT
Safety of SM-1500
Interventional
Factorial
Non-randomized
Open -no one is blinded
Uncontrolled
5
Treatment
Medicine | Device,equipment |
Single intrathecal infusion of KP-100IT at the low dose
Single intrathecal infusion of KP-100IT at the middle dose
Single intrathecal infusion of KP-100IT at the high dose
Multiple intrathecal infusion of KP-100IT
at the middle dose
Multiple intrathecal infusion of KP-100IT at the high dose
20 | years-old | <= |
65 | years-old | > |
Male and Female
- 'Clinically Definite ALS', 'Clinically Probable ALS' or 'Clinically Possible-Laboratory-supported ALS' by El Escorial Criteria
- Within 3 years after onset of the disease
- Stage I or II in ALS severity classification
-Have a serious disorder in any systems or have a serious metabolic defect, so that the investigators decide to be unsuitable for participation in the trial.
-Have hemoglobin A1c 6.1 (JDS value) or more.
-Any observation of diseases/symptomes below; malignant neoplasm, intrathecal infection/mass, proliferative retinopathy, %VC less than 70% in spirogram
-Have a history of intolerance to transplantation of medical devices
-Have received an investigational drugs or devices within a month before onformed consent
-Be unsuitable for participation in the trial for any reason, according to the investigators.
15
1st name | |
Middle name | |
Last name | Masashi Aoki, MD, PhD |
Touhoku University School of Medicine
Neurology
1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574 Japan
022-717-7189
aokim@med.tohoku.ac.jp
1st name | |
Middle name | |
Last name | Tetsushi Abe |
Kringle Pharma, Inc.
Department of Pharmaceutical Development
Saito Biotechnology Incubator, 7-7-15 Saito-Asagi, Ibaraki,, Osaka 560-0082 Japan
072-641-8739
http://www.kringle-pharma.com
info@kringle-pharma.com
Kringle Pharma, Inc.
Japan Agenct for MedicalResearch and Development
Other
Japan
None
None
NO
2011.6.3.、 初回
東北大学病院(宮城県)
2012 | Year | 01 | Month | 16 | Day |
Unpublished
Completed
2011 | Year | 09 | Month | 13 | Day |
2012 | Year | 01 | Month | 16 | Day |
2014 | Year | 08 | Month | 07 | Day |
2014 | Year | 08 | Month | 28 | Day |
2014 | Year | 09 | Month | 25 | Day |
2015 | Year | 08 | Month | 30 | Day |
2012 | Year | 01 | Month | 13 | Day |
2015 | Year | 07 | Month | 14 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007316