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Comprehensive Genomic Profiling and Next Generation Functional Drug Screening for Patients With Aggressive Haematological Malignancies

RECRUITINGSponsored by Medical University of Vienna
Actively Recruiting
SponsorMedical University of Vienna
Started2020-06-10
Est. completion2026-03-31
Eligibility
Age18 Years+
Healthy vol.Accepted

Summary

EXALT-2 is a prospective, randomized, three arm study for treatment decision guided either by either comprehensive genomic profiling, next generation drug screening or physician's choice

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

* patient is suffering from aggressive haematological disease AND has undergone at least two lines of previous therapies AND/OR has undergone at least one previous therapy and no standard treatment is available in the specific disease setting and disease specific guidelines recommend treatment in studies.
* duration of last response is less than 6 months defined as first day of last treatment to date of relapse, the response duration has to be available with dates (dd/mm/yyyy) for initiation of and relapse to previous treatment.
* best response to previous treatment has to be available.
* The patient is able to give written informed consent and wishes to undergo further therapy
* further therapy is medically feasible
* tumor cell-containing samples can be obtained

Exclusion Criteria:

* current participation in another experimental clinical trial
* performance status does not allow participation (ECOG ˃ 1)
* pregnancy, tested at screening
* patient suffers from classical or nodular, lymphocyte predominant Hodgkins lymphoma.
* other malignoma, diagnosed \<1a before inclusion (except localized squamous cell carcinoma of the skin, surgically curable melanoma of the skin, basal cell carcinoma of the skin)

Conditions6

Advanced LymphomaCancerRefractory Acute Myeloid LeukemiaRefractory LeukemiaRefractory LymphomaRefractory T-Cell Lymphoma

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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