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Biomolecular Analysis for Predicting Response to Regorafenib (RegoRec)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Completed

Conditions

Glioblastoma
Glioblastoma, IDH-wildtype

Treatments

Diagnostic Test: Biomolecular tumor analysis

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The study envisages NGS analysis on tumor tissue from patients treated with regorafenib for recurrent glioblastoma as per standard care, with the aim to identify predictive biomarkers for response.

Enrollment

53 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. recurrent glioblastoma after surgery and chemoradiation with temozolomide;
  2. indication to treatment with regorafenib per standard of care;
  3. written informed consent.

Exclusion criteria

None.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

53 participants in 1 patient group

Biomolecular tumor analysis
Other group
Description:
NGS, IHC, methylome and other molecular studies
Treatment:
Diagnostic Test: Biomolecular tumor analysis

Trial contacts and locations

1

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Central trial contact

Q. Giorgio D'Alessandris, MD; Silvia Chiesa, MD

Data sourced from clinicaltrials.gov

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