Recruiting
Phase 1

ADCE-T02

Sponsor:

Adcendo ApS

Code:

NCT06597721

Conditions

Advanced Solid Tumor

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

ADCE-T02

Study Details

Brief summary:

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.

Conditions

Advanced Solid Tumor

Study ID

NCT06597721

Start date

Nov 25, 2024

Status verified date

Jul, 2026

Completion date

Jun 30, 2027

Anticipated

Primary completion date

Mar 30, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Patients must have pathologically confirmed unresectable advanced solid tumor
2. Patients who have undergone at least one systemic therapy and have progressive disease
3. Patients must have at least one measurable lesion as per RECIST version 1.1.
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
5. Life expectancy ≥ 3 months.
6. Patients must have adequate organ function as indicated by laboratory values
7. Women of childbearing potential (WCBP), defined as sexually mature women who have not undergone surgical sterilization or who have not been naturally postmenopausal for at least 12 consecutive months must agree to use two effective contraceptive methods while on study treatment and for at least 7 months after the last dose of ADCE T02.
8. Male patients must agree to use condoms, even if they have had a successful vasectomy, while on study treatment and for at least 4 months after the last dose of ADCE T02.

Key Exclusion Criteria:

1. Prior treatment with any agent targeting Tissue Factor or any ADC with a topoisomerase 1 payload
2. Central nervous system (CNS) metastasis.
3. Active ocular surface disease or a history of cicatricial conjunctivitis or inflammatory conditions that predispose to cicatrizing conjunctivitis, mucus pemphigoid or penetrating ocular transplants.
4. Persistent toxicities from previous systemic anti-neoplastic treatments
5. Known past or current coagulation defects leading to an increased risk of bleeding
6. Significant cardiac disease; recent myocardial infarction, acute coronary syndromes, congestive heart failure, uncontrolled hypertension, uncontrolled cardiac arrhythmias
7. History of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required steroids, or current ILD/pneumonitis, or suspected ILD/pneumonitis
8. Prior second malignancy except for:

  • Well treated basal cell carcinoma or squamous cell carcinoma of the skin.
  • Low-risk prostate cancer with a Gleason score < 7 and a PSA level < 10 ng/mL
  • Any cancer or in situ cancer the patient has been disease-free for ≥ 2 years.

Study Design

Enrollment

210 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: ADCE-T02 Dose Escalation followed by an Expansion Phase

Interventions

ADCE-T02

Administered intravenously

Primary outcome measure

  • Maximum Tolerated Dose (MTD) of ADCE-T02 [ Time Frame: Up to 24 months ]
  • Recommended Expansion Phase Dose (RED) of ADCE-T02 [ Time Frame: Up to 24 months ]
  • Type, incidence and severity of Adverse Events [ Time Frame: Up to 24 months ]

Central Contacts and Locations

Central contacts

Locations

Highlands Oncology Group

Recruiting

Rogers, Arkansas, United States, 72758

Yale University Cancer Center

Recruiting

New Haven, Connecticut, United States, 06520

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02114

MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

START San Antonio

Recruiting

San Antonio, Texas, United States, 78229

More Information

Sponsor

Adcendo ApS

Last update posted

Jul 15, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Adcendo ApS on 2026-07-15.