General information
  • Disease category Leukemia (BASEC)
  • Recruitment status recruitment ongoing (BASEC/ICTRP)
  • Trial sites
    Zurich
    (BASEC)
  • Contact Cornelia Baumgartner cornelia@t-curx.com (BASEC)
  • Data Source(s) BASEC: Import from 07.09.2026 ICTRP: N/A
  • Last update 07.09.2026 16:10
HumRes68132 | SNCTP000006901 | BASEC2026-00192

A first clinical study in humans using the patient's own T-cells that carry a special receptor against a protein called Siglec-6, in cases of hard-to-treat or recurrent acute myeloid leukemia or chronic lymphocytic leukemia

  • Disease category Leukemia (BASEC)
  • Recruitment status recruitment ongoing (BASEC/ICTRP)
  • Trial sites
    Zurich
    (BASEC)
  • Contact Cornelia Baumgartner cornelia@t-curx.com (BASEC)
  • Data Source(s) BASEC: Import from 07.09.2026 ICTRP: N/A
  • Last update 07.09.2026 16:10

Summary description of the study

TCX-001 is a novel, personalized therapy in which the patient's own immune cells (T-cells) are processed in the laboratory and equipped with a special receptor. This receptor recognizes the surface marker Siglec-6 on cancer cells and specifically targets them.
Early laboratory studies show that TCX-001 can specifically recognize and kill cancer cells in AML and CLL. In this study, a protein called Siglec-6 is being clinically tested in humans for the first time as a target molecule. The aim is to investigate whether treatment with TCX-001 is safe and whether early signs of efficacy can be observed in patients with limited treatment options.
The main objective of this study is to evaluate the safety of TCX-001 and to determine the maximum tolerated dose (MTD) or the recommended dose for Phase 2 (RP2D).
The study is divided into two sections:
In the first section, the treatment will initially be tested with two very low doses:
• Level 1: 100,000 CAR-T cells per kilogram of body weight
• Level 2: 300,000 CAR-T cells per kilogram of body weight
Each dosage starts with a so-called "sentinel patient," meaning that initially, a single patient is treated and closely monitored over a specified period before additional patients are included.
In the second phase, the dose will be gradually increased depending on how well TCX-001 is tolerated. The planned dosages are:
• Level 3: 1 million CAR-T cells per kilogram of body weight
• Level 4: 3 million CAR-T cells per kilogram
• Level 5: 6 million CAR-T cells per kilogram
Patients will be treated in groups of three. A standardized procedure will be used for dose finding to identify a suitable dose at which no more than 30% of patients experience serious side effects.
Whether the dose is increased or maintained will be decided by an independent committee of investigators and a statistician.

(BASEC)

Intervention under investigation

This study investigates whether the investigational drug TCX-001, when administered once intravenously, is safe, well tolerated, and can be used for the treatment of AML or CLL.
The investigational drug TCX-001 consists of the patient's own, genetically modified white blood cells from the immune system (T-cells) that are equipped with a protein complex known as a chimeric antigen receptor (CAR). These T-cells are also called CAR-T cells. The CAR protein complex recognizes a protein structure on other body cells with the scientific name Siglec-6. Current knowledge indicates that Siglec-6 is present on the surface of AML and CLL cancer cells, as well as on a few healthy cells, such as certain immune system defense cells (B-cells, basophilic granulocytes, mast cells). With the help of the CAR protein complex, CAR-T cells bind to Siglec-6 and can neutralize AML and CLL cancer cells. TCX-001 is manufactured from the participant's own T-cells.

(BASEC)

Disease under investigation

acute myeloid leukemia (AML);
chronic lymphocytic leukemia (CLL)

(BASEC)

Criteria for participation in trial

1. At least 18 years old
2. Life expectancy of at least 3 months
3. Adequate kidney, liver, and heart function

(BASEC)


Exclusion criteria

1. Stem cell transplantation within the last 3 months or active GvHD with systemic immunosuppression
2. Any other active cancer in the last 2 years (except for locally treated cancer)
3. Active infection or other serious illness

(BASEC)

Trial sites

Zurich

(BASEC)

not available

Sponsor

Sponsor: T-CURX GmbH Sponsor’s representative: Maxia Strategies LLC

(BASEC)

Contact

Contact Person Switzerland

Cornelia Baumgartner

+41 78 913 06 38

cornelia@t-curx.com

T-CURX GmbH Friedrich-Bergius-Ring 15 97076 Würzburg Deutschland

(BASEC)

Scientific Information

not available

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Zurich

(BASEC)

Date of authorisation

08.05.2026

(BASEC)


ICTRP Trial ID
not available

Official title (approved by ethics committee)
A phase 1, first-in-human study evaluating the safety, tolerability, and efficacy of autologous T-cells carrying a Siglec-6-specific chimeric antigen receptor (CAR) in adult patients with Refractory or Relapsed (RR) Acute Myeloid Leukemia (AML) or Chronic Lymphocytic Leukemia (CLL) (BASEC)

Academic title
not available

Public title
not available

Disease under investigation
not available

Intervention under investigation
not available

Type of trial
not available

Trial design
not available

Inclusion/Exclusion criteria
not available

not available

Primary and secondary end points
not available

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
not available

Secondary trial IDs
not available

Results-Individual Participant Data (IPD)
not available

Further information on the trial
not available

Results of the trial

Results summary

not available

Link to the results in the primary register

not available