Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GLB-007 is a preclinical molecular glue degrader (MGD) developed by Hangzhou GluBio Pharmaceutical for the treatment of sickle cell disease and beta-thalassemia. It functions by inducing the proteasomal degradation of WIZ (Widely Interspaced Zinc Finger Motifs) and ZBTB7A (Zinc finger and BTB domain-containing protein 7A), which are key transcriptional repressors of fetal hemoglobin (HbF). By eliminating these repressors, GLB-007 promotes the reactivation of HbF production, which can compensate for the defective or missing adult hemoglobin in patients with these genetic blood disorders. This small-molecule approach aims to provide a potentially more accessible, oral alternative to current gene therapy treatments for hemoglobinopathies.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on GLB-007.