ADCE-T02
DrugAdministered intravenously
NCT Number: NCT06597721
Adcendo ApS is conducting a phase 1 study of an investigational drug called ADCE-T02 (previously known as AMT-754), a tissue factor targeted antibody-drug conjugate which may be used in the future as a possible treatment for advanced solid tumors.
The main purpose of the study is to determine the Maximum Tolerated Dose (MTD), the recommended dose and the safety and tolerability of ADCE-T02 when given as a single therapy over a range of different dose levels.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Macquarie University Hospital, Macquarie Park, New South Wales, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Administered intravenously
Time frame: Up to 24 months
The MTD will be determined using DLTs
Time frame: Up to 24 months
The RED will be determined using dose limiting toxicities (DLTs) and all other available study data
Time frame: Up to 24 months
Safety and tolerability profile of ADCE-T02 assessed by the Common Terminology Criteria for Adverse Events v5.0
Time frame: Up to 24 months
Proportion of patients achieving Complete Response (CR) or Partial Response (PR)
Time frame: Up to 24 months
Proportion of patients achieving CR, PR or Stable Disease (SD)
Time frame: Up to 24 months
Time from date of start of treatment to date of the first progression or death, whichever occurs first.
Time frame: Up to 24 months
Immunogenicity profile characterized by concentration of ADAs
Time frame: Up to 24 months
Pharmacokinetic profile characterized by the maximum observed concentration (C[max]) of ADCE-T02
Time frame: Up to 24 months
Pharmacokinetic profile characterized by the area under the curve (AUC) of ADCE-T02
Time frame: Up to 24 months
Pharmacokinetic profile characterized by the terminal half-life (t[1/2]) of ADCE-T02
Time frame: Up to 24 months
Pharmacokinetic profile characterized by the time to maximum concentration (Tmax)
Contact information is provided by the study sponsor or research team.
Adcendo ApS
Industry
First-in-Human, Phase 1 Study of ADCE-T02, a Tissue Factor Targeted Antibody-Drug Conjugate, in Patients With Advanced Solid Tumors
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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