Clinical Trial Details
— Status: No longer available
Administrative data
NCT number |
NCT03624842 |
Other study ID # |
CTDH-AD-EA-001 |
Secondary ID |
|
Status |
No longer available |
Phase |
|
First received |
|
Last updated |
|
Study information
Verified date |
August 2018 |
Source |
CTD Holdings, Inc. |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Expanded Access
|
Clinical Trial Summary
To afford urgent access to a potential-disease modifying treatment, Dr. Diana Kerwin, in
partnership with CTD Holdings, the manufacturer of Trappsol (R) Cyclo(TM), will administer
the product to a patient with Alzheimer's Disease who has no other disease-modifying
treatment options.
Description:
Trappsol(R) Cyclo(TM) will be administered via intravenous (IV) infusion. The initial dose
will be 500 mg/kg (T=Day 0). Subsequent dosing is anticipated to increase over 9 months, with
all subsequent doses given monthly at the maximum dose determined by tolerability, lack of
toxicity or adverse event, pharmacokinetic analysis and patient preference. So long as the
overall risk/benefit profile favors continued dosing, the patient will continue to receive
Trappsol (R) Cyclo (TM) for a minimum of 12 months, if not perpetually.
Risk/benefit assessments will include:
- Vital signs, ECG and laboratory parameters (CBC, chemistry panel, hematology,
urinalysis, lipids, coagulation)
- Brain MRI without gadolinium for safety monitoring
- Amyloid and Tau PET (positron emission tomorgraphy) imaging
- Adverse Events
- Mini-mental status score
- Digital Cognition Technologies (DCT) Clock
- Changes in blood biomarkers
- Pharmacokinetic data