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. 2023 Aug 8;7(Suppl):e87048d4. doi: 10.1097/01.HS9.0000970996.87048.d4

P1024: MYLOX-1: A PHASE II STUDY EVALUATING THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF ORAL LOXL2 INHIBITOR GB2064 (WITH FOCUS ON BONE MARROW COLLAGEN) IN PATIENTS WITH MYELOFIBROSIS

Claire Harrison 1, John Mascarenhas 2, Daniela Cilloni 3, Richard Schlenk 4, Brian Jacoby 5, Robert J Slack 6, Vassilios Aslanis 7, Bhupinder Singh 8, Bertil Lindmark 9, Srdan Verstovsek 10, Raajit K Rampal 11
PMCID: PMC10431423

Abstract Topic: 16. Myeloproliferative neoplasms - Clinical

Background: Myelofibrosis (MF) treatment (Tx) with Janus kinase (JAK) inhibitors is limited by modest effects on bone marrow (BM) fibrosis & driver mutation allele burden. A high proportion of patients (pts) discontinue Tx due to cytopenias. GB2064, a LOXL2 inhibitor, is being developed as a potential disease-modifying Tx for MF.

Aims: To evaluate safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) & clinical effects, specifically potential effects on BM collagen fibrosis, of oral GB2064 in pts with primary or secondary MF (PMF/SMF).

Methods: MYLOX-1 (NCT04679870) is a phase II trial of oral GB2064 (1000 mg BID) administered in pts with PMF/SMF for 9 months, with follow-up 1 month after their last dose. Eligible pts were not allowed JAK inhibitors, had clinical laboratory parameters within protocol-defined limits & an ECOG performance status of 0–2. Primary endpoints: Safety & tolerability. Clinical visits occurred at protocol-specified timepoints: safety & tolerability, PK, PD & appropriate MF-specific assessments occurred at all visits except on Day (D) 7, D15 & Month (M) 4, when only safety & tolerability were assessed. BM biopsies & MRI of the spleen were performed at baseline & M3, M6 & M9. Pts who showed clinical benefit entered an extension phase & may continue Tx for an additional 3 years, during which only safety & tolerability are assessed.

Results: As of early February 2023, 17 pts have been enrolled & started Tx (59% PMF); 10 JAK2 positive (3 with co-existing ASXL1 mutations, 1 with co-existing MPL & ASXL1 mutations), 2 MPL positive, 4 CALR positive (1 with co-existing EZH2 mutation) & 1 ASXL1 positive. JAK2 inhibitor status: 4 refractory, 8 intolerant, 2 ineligible, 3 naïve. Dynamic International Prognostic Scoring System plus risk distribution: High for 2 pts, Intermediate-2 for 8, Intermediate-1 for 5 & Low for 2. Overall, 6 pts have completed Tx (2 are in the extension phase), 10 have discontinued Tx (6 due to adverse events [AEs], 3 due to disease progression) & 1 is continuing Tx.

At the safety data cut-off (6 October 2022), all pts who received GB2064 experienced Tx-emergent AEs. Most were gastrointestinal in nature (11/16 pts), including nausea (6/16 pts) & vomiting (3/16 pts), & were either self-limiting or responded to anti-emetics. Serious AEs were experienced by 7 pts, 1 was Tx related (fall).

Of 5 evaluable pts who received GB2064 for >6 months & had complete BM biopsy data, 1 (20%) showed improved ≥1-grade reticulin fibrosis, & 4 (80%) experienced a 1- or 2 grade reduction in collagen fibrosis (Figure). Spleen volume & hematological parameters remained stable from baseline to M6 for the 4 pts with BM collagen fibrosis response; none required transfusion. After M6 assessments, 2/4 pts progressed to the extension phase due to clinical benefit seen with GB2064 (1 experienced a total symptom score reduction >50% & the other an Anemia response).

BM penetration by GB2064 was demonstrated through spatial distribution in M3 BM biopsies using matrix-assisted laser desorption/ionization mass spectrometry imaging. GB2064 showed good target engagement in plasma, with a 49.5% decrease in free LOXL2 from baseline to 2 hours post-dosing.

Summary/Conclusion: Pts with MF who received GB2064 had an acceptable safety profile & improvements in BM reticulin & collagen fibrosis that indicated disease-modifying activity. GB2064 demonstrated BM penetration & good target engagement in plasma, thus may be a valid Tx option or disease-modifying combination agent for pts ineligible or intolerant to JAK inhibitors, or in combination with JAK inhibitors & novel therapies.

Figure:

graphic file with name hs9-7-e87048d4-g001.jpg

Keywords: Clinical trial, Bone Marrow Fibrosis, Myelofibrosis, Janus Kinase inhibitor


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