Exposition of humans with TMDD
Conditions
Interventions
Group 1: Single oral dosage 0,075 mg/kg bw
Single dermal dosage 0,75 mg/kg bw of a solution containing 5% TMDD
Sponsors
Verband der Chemischen Industrie e.V.
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Healthy
Exclusion criteria
Exclusion criteria: Allergic persons expectant mothers breast-feeding mothers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of major metabolites of TMDD in human urine | — |
Secondary
| Measure | Time frame |
|---|---|
| Toxicokinetics of the test compound and its major metabolites. By means of urine samples within 72 h after application | — |
Countries
Germany
Contacts
Public ContactGerhard Scherer
ABF Analytisch-Biologisches Forschungslabor GmbH
Outcome results
None listed