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(Bispecific) Antibodies in Cancer Patients

(Bispecific) Antibodies in Cancer Patients (InHeAb01)

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05119257
Acronym
InHeAb01
Enrollment
Unknown
Registered
2021-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Brief summary

The aim of this project is to provide (bispecific) antibodies to individual patients with advanced solid and hematological malignancies without any available approved treatment options.

Detailed description

Ethics: Patient treatment will be conducted according to §13 Absatz 2b, AMG (German law). All (bispecific antibodies) applied are developed and manufactured by the principle investigator Prof. Helmut Salih.

Interventions

BIOLOGICALBispecific antibodies (bsAB)

BsAbs equipped with a target-specificity directed to a TAA and an effector-specificity for an activating receptor on T cells, such as CD3 or CD28, are applied intravenously in repeated cycles until disease progression or dose limiting toxicity.

Sponsors

University Hospital Tuebingen
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Documented diagnosis of advanced malignant disease * Advanced malignant disease without any available standard of care treatment option * Live expectancy \> 3 month * Ability to understand and voluntarily sign an informed consent form. * Ability to adhere to the visit schedule and other protocol requirements * Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 2.

Exclusion criteria

* Pregnant or lactating females. * Treatment regimens inducing severe T cell deficiencies * Treatment-related side effect from prior cancer treatment \> CTC grade 2 (CTCAE V5.0) * Participation in any clinical study or having taken any investigational therapy, which would interfere with the studys primary and secondary end points within 2 weeks prior to Ab treatment.

Countries

Germany

Contacts

Primary ContactHelmut R. Salih, Prof.
helmut.salih@med.uni-tuebingen.de+497071/2983275

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026