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Exicure to Present Data from Burixafor Phase 2 Trial at the 2026 Tandem Meetings

Key Takeaway: Exicure, Inc. will present data from its Phase 2 trial of burixafor at the 2026 Tandem Meetings. The trial evaluated burixafor's effectiveness in mobilizing hematopoietic progenitor cells for patients with multiple myeloma undergoing autologous transplantation. The study reported a high success rate in achieving the primary endpoint, highlighting burixafor's potential as a reliable mobilization strategy.
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POSITIVE FACTORS

  • Successful presentation of Phase 2 trial data at a major conference.
  • High percentage (89.7%) of patients met the primary endpoint.
  • Burixafor offers a reliable mobilization strategy for stem cell collection.
  • Combination therapy shows a favorable safety profile.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+35%
120-day peak, hindsight
Typical move
25%
average across 2 past catalysts
Cash runway
~5 mo
High dilution risk
Lead asset
TG-0054 combined with G-CSF
Phase 2 · Multiple Myeloma

Full Press Release Details

REDWOOD CITY, Calif., Jan. 21, 2026 (GLOBE NEWSWIRE) -- Exicure, Inc. (Nasdaq: XCUR), a clinical-stage biotechnology company developing therapeutics for hematologic diseases, today announced that it will present a poster at the upcoming 2026 Tandem Meetings | Transplantation & Cellular Therapy Meetings of the American Society for Transplantation and Cellular Therapy (ASTCT) and Center for International Blood and Marrow Transplant Research (CIBMTR), taking place February 4-7, 2026, in Salt Lake City, UT.
The presentation will serve as an encore of data reported previously, highlighting results from Exicure’s open-label, multicenter Phase 2 trial (NCT05561751) evaluating burixafor in patients with multiple myeloma undergoing autologous hematopoietic cell transplantation (AHCT). Exicure recently sharedpositive topline data from the trial, which assessed burixafor’s ability to mobilize hematopoietic progenitor cells by blocking CXCR4, a chemokine receptor that plays a central role in retaining hematopoietic stem cells in the bone marrow niche. Blockade of this pathway facilitates stem cell movement from the bone marrow into the peripheral blood for collection and use in transplantation procedures.
“Effective stem cell mobilization remains a challenge for patients with multiple myeloma undergoing autologous transplantation, particularly in the modern treatment era where exposure to lenalidomide- and daratumumab-based induction is common and mobilization options are limited,” said Yosra Aljawai, M.D., a lead investigator, poster presenter and Assistant Professor, Department of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center. “In our Phase 2 study, burixafor in combination with propranolol and G-CSF provided reliable mobilization and a favorable safety profile. 89.7% of the patients successfully met the primary endpoint, with the added advantage of same-day administration and leukapheresis. This offers an important alternative collection strategy for patients who may face barriers to successful stem cell collection.”
Poster Presentation DetailsAbstract Number:29283Title:An Open-Label, Multi-Center Phase 2 study to Assess the Safety and Efficacy of Burixafor (GPC-100) and Propranolol with G-CSF for the Mobilization of Hematopoietic Progenitor Cells in Patients with Multiple MyelomaPresenter:Dr. Yosra Aljawai, Assistant Professor, Department of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer CenterSession:Graft sources, mobilization, donor safety.Date and Time:February 5, 2026, 6:30 PM
About ExicureExicure, Inc. (Nasdaq: XCUR) is a clinical-stage biotechnology company developing therapies to address key challenges in hematologic diseases. The company’s lead program, burixafor (GPC-100), is a highly selective small molecule antagonist of CXCR4, a chemokine receptor that plays a central role in retaining hematopoietic stem cells in the bone marrow niche. By blocking CXCR4, burixafor may enhance stem cell mobilization into the peripheral blood to support collection and use in autologous hematopoietic cell transplantation (AHCT).
Burixafor is being evaluated for its potential to improve stem cell mobilization in multiple myeloma, sickle cell disease, and in support of cell and gene therapy. In addition, Exicure is planning a chemosensitization trial in acute myeloid leukemia (AML), leveraging burixafor’s ability to mobilize malignant cells from protective bone marrow niches into the peripheral blood, where they may be more effectively targeted by chemotherapy. Burixafor became part of Exicure’s pipeline following the company’s acquisition of GPCR Therapeutics, Inc. in January 2025. For more information, visitwww.exicuretx.com.

Media Contact:Sarah Ellinwood, PhDKendall Investor Relationssellinwood@kendallir.com

Frequently Asked Questions

What is the focus of Exicure's Phase 2 trial?

The trial focuses on evaluating burixafor's effectiveness in mobilizing hematopoietic progenitor cells in multiple myeloma patients.

When will Exicure present its trial data?

Exicure will present its trial data at the 2026 Tandem Meetings from February 4-7, 2026.

What was the success rate of the primary endpoint?

The trial reported a success rate of 89.7% in meeting the primary endpoint.

What is burixafor's mechanism of action?

Burixafor blocks the CXCR4 receptor, facilitating the movement of stem cells from the bone marrow.

Last updated: Jan 21, 2026