X4 Pharmaceuticals Presents New Clinical Data at ASH 2021 Further Supporting Potential of Mavorixafor + Ibrutinib to Treat Patients with Double-Mutation Waldenström’s Macroglobulinemia

Rhea-AI Summary

X4 Pharmaceuticals (Nasdaq: XFOR) announced positive interim results from its ongoing Phase 1b trial of mavorixafor in combination with ibrutinib for patients with Waldenström’s macroglobulinemia (WM) and specific mutations. The trial has achieved a remarkable 100% overall response rate in evaluable patients. After 12 months, patients saw significant reductions in serum IgM levels, with median decreases from 47.2 g/L to 7.73 g/L. Further data, including responses from refractory patients, is expected throughout 2022.

Positive

• 100% overall response rate in evaluable patients.
• Median serum IgM reduced significantly from 47.2 g/L to 7.73 g/L after 12 months.
• Combination therapy showed promising results in refractory patients compared to previous studies.

Negative

• None.

- CXCR4 antagonism proof of concept established, with 100% overall response rate to combination treatment in frontline and refractory patients -

- Median Serum IgM reductions in refractory CXCR4^MUT patients on combination therapy similar to those seen in CXCR4^WT patients on ibrutinib monotherapy -

- Study enrollment ongoing at highest dose of mavorixafor; longer-term response data, dose selection, and regulatory updates expected in 2022 -

BOSTON, Dec. 11, 2021 (GLOBE NEWSWIRE) -- X4 Pharmaceuticals, Inc. (Nasdaq: XFOR), a leader in the discovery and development of novel CXCR4-targeted small molecule therapeutics to benefit people with immune system dysfunction, today announced new positive efficacy and safety data from the ongoing Phase 1b clinical trial of its lead candidate mavorixafor, in combination with ibrutinib, for patients with Waldenström’s macroglobulinemia (WM) and confirmed MYD88 and CXCR4 mutations. These study results were reported today in a poster presentation at the American Society of Hematology (ASH) Annual Meeting, taking place both virtually and in person in Atlanta, GA, December 11-14, 2021.

“We continue to be excited by the data from our ongoing Phase 1b clinical trial, with 100% of evaluable patients achieving an overall response (OR) to date,” said Diego Cadavid, M.D., Chief Medical Officer of X4 Pharmaceuticals. “In addition, when looking at the refractory sub-population of patients within the study, the interim data suggest that serum IgM responses in these double-mutation patients are greater with the combination treatment than with ibrutinib alone in previous studies. Importantly, we believe that these results support the premise that CXCR4 antagonism can eliminate some or all of the negative impacts of CXCR4 mutations in this higher-risk sub-population of Waldenstrom’s patients.” Dr. Cadavid concluded: “We look forward to reporting further data from this trial and from ongoing pre-clinical research studies throughout 2022, as we continue to explore the potential of mavorixafor across broader lymphoma patient populations and in additional treatment combinations.”

Steven Treon, M.D., Ph.D., FACP, FRCP, Director of the Bing Center for Waldenström's Macroglobulinemia at Dana-Farber Cancer Institute, Professor of Medicine at Harvard Medical School, and the poster’s lead author commented: “The interim data from this investigational study continue to look promising, with the combination therapy leading to rapid, clinically meaningful, and durable decreases in serum IgM levels and increases in hemoglobin in these difficult-to-treat double-mutation patients, to date.”

What’s New in This Poster?

• As of October 12, 2021, 16 patients were enrolled in the Phase 1b clinical trial, with 14 being evaluable as of the data cut, all at low- (200 mg) and mid-level (400 mg) dosing of mavorixafor; median duration of treatment was 272.5 days (range 33-435 days); 12 patients remain on study.
  

For all patients on study (both frontline and refractory):

• The median level of serum IgM reduced from 47.2 g/L (N=14) at baseline to 7.73 g/L (N=3) after 12 months of treatment.
• In 10 patients evaluable for response, the overall response rate was 100% (ORR = >25% reduction in serum IgM), with four achieving a Major Response (>50% reduction in serum IgM), including one Very Good Partial Response (VGPR) of >90% reduction in serum IgM.
• The median level of hemoglobin approached normal, increasing by approximately 38 g/L from baseline (N=14) to month 12 (N=3).
• Overall, the combination of mavorixafor and ibrutinib was tolerated with a manageable safety profile at the low- and mid-level dosing of mavorixafor; dose escalation to 600 mg mavorixafor is ongoing.

For patients with refractory disease:

• Median decreases in serum IgM from 50.2 g/L at baseline (N=8) to 7.7 g/L at 12 months (N=3) were similar to decreases seen in a previous study of ibrutinib monotherapy in Waldenström’s patients without CXCR4 mutations.
• An ORR of 100% (N=7), with two achieving a Major Response, including one VGPR, was seen.
• Median time-on-treatment for patients achieving a Major Response was 51.7 weeks (N=3); median time on treatment for patients achieving Minor Responses (MR = 25% to <50% reduction in serum IgM) was 30.1 weeks (N=4).
• The median level of hemoglobin approached normal, increasing by approximately 32 g/L from baseline (N=18) to month 12 (N=1).

About Waldenström’s Macroglobulinemia and Associated CXCR4 Mutations
Waldenström’s macroglobulinemia is a rare B-cell lymphoproliferative disorder characterized by increased immunoglobulin M (IgM). Greater than 90% of patients with Waldenström’s have acquired mutations in the MYD88 gene, with a subset (30%–40%) also having mutations in chemokine receptor CXCR4. The presence of the CXCR4 mutation is associated with greater cancer burden, higher serum IgM levels, and increased risk of developing a serious emergent condition called symptomatic hyperviscosity syndrome. Importantly, the presence of CXCR4 mutations has been shown to negatively impact patients’ response to ibrutinib (a BTK inhibitor), as manifested by delayed response, inferior depth of response, and/or shorter progression-free survival.

About Mavorixafor and the Phase1b Clinical Trial in Waldenström’s Macroglobulinemia
Mavorixafor is an oral small-molecule antagonist of the CXCR4 receptor with a demonstrated ability to inhibit binding of its ligand, CXCL12; this inhibition of CXCR4 has been shown to sensitize Waldenström’s cells with both MYD88 and CXCR4 mutations to BTK antagonists, such as ibrutinib. The ongoing Phase 1b, open-label, multicenter, single-arm study (NCT04274738) examines intra-patient dose escalation, safety, pharmacokinetics, and pharmacodynamics of mavorixafor in combination with ibrutinib in up to 18 patients aged 18 years or older with a diagnosis of Waldenström’s macroglobulinemia and confirmed MYD88 and CXCR4 genetic mutations. In the study, all cohorts are dosed with oral, once-daily doses of ibrutinib 420 mg. In Cohorts A and B, patients are initiated on oral, once-daily mavorixafor 200 mg (low dose) and are escalated to 400 mg mavorixafor (mid-dose) after 28 days if no dose-limiting toxicities are observed in five of six participants. Patients in Cohort C are initiated at 400 mg mavorixafor. Participants are escalated to 600 mg mavorixafor (high dose) after 400 mg is deemed tolerable. All patients are followed for adverse events and change from baseline in serum IgM and hemoglobin, pharmacokinetics, and pharmacodynamic markers, including peripheral white blood cell counts (WBCs) and clinical response.

About X4 Pharmaceuticals
X4 Pharmaceuticals is a late-stage clinical biopharmaceutical company leading the discovery and development of novel therapeutics to benefit people with immune system dysfunction. The company’s lead candidate is mavorixafor, a first-in-class, small molecule antagonist of chemokine receptor CXCR4 that is being developed as a once-daily oral therapy. Due to mavorixafor’s ability to antagonize CXCR4 and improve the healthy maturation and trafficking of white blood cells, X4 believes that mavorixafor has the potential to provide therapeutic benefit across a wide variety of diseases, including primary immunodeficiencies (PIDs) and certain types of cancer. Mavorixafor has already demonstrated clinical potential in a Phase 2 trial in people with WHIM syndrome, a rare PID. Its efficacy and safety continue to be evaluated in a global Phase 3 clinical trial in WHIM (fully enrolled) and in two Phase 1b clinical trials – one, as monotherapy in people with Severe Congenital Neutropenia (SCN) and other chronic neutropenia conditions, and another in combination with ibrutinib in people with Waldenström’s macroglobulinemia, a rare B-cell lymphoma. X4 is continuing to leverage its insights into CXCR4 biology at its corporate headquarters in Boston, Massachusetts and at its research facility in Vienna, Austria, to discover and develop additional product candidates. For more information, please visit www.x4pharma.com.

Forward Looking Statements:
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. These statements may be identified by the words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target,” or other similar terms or expressions that concern X4's expectations, strategy, plans, or intentions. Forward-looking statements include, without limitation, statements regarding the clinical development and therapeutic potential of mavorixafor and the advancement of X4’s pipeline. Any forward-looking statements in this press release are based on management's current expectations and beliefs. Actual events or results may differ materially from those expressed or implied by any forward-looking statements contained herein, including, without limitation, uncertainties inherent in the initiation and completion of preclinical studies and clinical trials and clinical development; the risk that trials and studies may be delayed, including, but not limited to, as a result of the effects of the ongoing COVID-19 pandemic or delayed patient enrollment, and may not have satisfactory outcomes; the risk that the outcomes of preclinical studies or earlier clinical trials will not be predictive of later clinical trial results; the potential adverse effects arising from the testing or use of mavorixafor or other product candidates; risks related to X4’s ability to raise additional capital and other risks and uncertainties, including those described in the section entitled “Risk Factors” in X4’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) on November 4, 2021, and in other filings X4 makes with the SEC from time to time. X4 undertakes no obligation to update the information contained in this press release to reflect new events or circumstances, except as required by law.

Contacts:

Glenn Schulman, PharmD, MPH (corporate)
VP, Investor Relations & Corporate Communications
glenn.schulman@x4pharma.com
(203) 494-7411

Daniel Ferry (investors)
Managing Director, LifeSci Advisors
daniel@lifesciadvisors.com
(617) 430-7576

Mónica Rouco Molina (media)
Senior Account Executive, LifeSci Communications
mroucomolina@lifescicomms.com

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/4e5fbf54-18ea-4901-a6e5-154c2a996e75

FAQ

What were the results of the XFOR Phase 1b trial presented on December 11, 2021?

The Phase 1b trial showed a 100% overall response rate in evaluable patients, with median serum IgM levels decreasing significantly.

What is the significance of mavorixafor in treating Waldenström’s macroglobulinemia?

Mavorixafor is a novel CXCR4 antagonist that, in combination with ibrutinib, targets patients with specific genetic mutations and has demonstrated superior efficacy.

When can we expect further data from X4 Pharmaceuticals regarding mavorixafor?

Further data and regulatory updates from the ongoing study are expected throughout 2022, specifically on longer-term responses.

What is the target patient population for the mavorixafor trial?

The trial targets patients with Waldenström’s macroglobulinemia and confirmed MYD88 and CXCR4 mutations.