TJ Biopharma Announces Publication of Plonmarlimab Phase 2 Results in the Journal of Hematology & Oncology

• Findings build on TJ Biopharma's pioneering work on GM-CSF as a therapeutic target in macrophage- and myeloid cell-driven inflammation
• Phase 2 results show encouraging clinical responses and glucocorticoid-sparing potential in macrophage activation syndrome

HANGZHOU, China, Nov. 4, 2026 /PRNewswire/ -- TJ Biopharma ("TJ Bio" or "the Company"), a fully integrated biotech company focusing on discovery, development, manufacturing and commercialization of innovative biologics in the areas of autoimmune diseases, oncology and metabolic disorders, today announced the publication of results from PRIME-1, a Phase 2 study of plonmarlimab in macrophage activation syndrome (MAS), in the Journal of Hematology & Oncology. Plonmarlimab is the Company's internally developed monoclonal antibody targeting GM-CSF.

PRIME-1 is an open-label, single-arm, multi-center Phase 2 study designed to evaluate the efficacy, safety, tolerability, pharmacokinetics and immunogenicity of plonmarlimab in patients with MAS. The findings showed encouraging clinical responses with a rapid onset of response and the potential to substantially reduce glucocorticoid use, providing further clinical evidence to support targeting GM-CSF in MAS.

MAS is a life-threatening hyperinflammatory condition that may arise as a complication of a range of autoimmune rheumatic diseases. Published reports from China indicate that only approximately 40% of patients respond to first-line glucocorticoid therapy, while mortality in patients with relapsed or refractory MAS can exceed 60%. With no therapies currently approved specifically for MAS in China, substantial unmet medical needs remain.

The published study enrolled 18 patients with MAS who were refractory to or had relapsed after high-dose glucocorticoid therapy. Key findings included:

• 83.3% overall response rate at Week 8: 15 of 18 patients achieved a complete or partial response.
• Median time to response of 2.1 weeks: The earliest response was observed on Day 5 of treatment.
• 79.3% reduction in glucocorticoid dose: The least-squares mean percentage reduction from baseline was 79.3% at Week 8, with 83.3% of patients achieving a dose reduction of at least 50%.
• Well tolerated safety profile: No Grade 3 or higher infections were observed, and no adverse events led to permanent treatment discontinuation or death during the study.

"MAS can progress rapidly and become life-threatening, making prompt control of excessive inflammation critical," said Professor Zhao Wang of the Department of Hematology at Beijing Friendship Hospital, Capital Medical University, and a co-corresponding author of the publication. "The encouraging and relatively rapid clinical responses observed in patients who had responded inadequately to prior treatment provide preliminary clinical evidence supporting the potential of GM-CSF-targeted therapy in MAS."

"MAS is a serious complication of several autoimmune rheumatic diseases, and its treatment remains challenging," said Professor Qiong Fu of the Department of Rheumatology and Immunology at Renji Hospital, Shanghai Jiao Tong University School of Medicine, and a co-corresponding author of the publication. "Alongside encouraging clinical responses, the study showed the potential for substantial reductions in glucocorticoid use. These findings warrant further investigation, and we look forward to their validation in subsequent studies."

Plonmarlimab has received Breakthrough Therapy Designation from the Center for Drug Evaluation (CDE) of China's National Medical Products Administration (NMPA) for MAS. The publication of the Phase 2 results and initiation of a Phase 3 study mark continued progress in its clinical development. The Company is also conducting PRIME-2, a Phase 2 study in gouty arthritis, and has received investigational new drug (IND) clearance to initiate PRIME-3, a Phase 2 study in sepsis.

"Publication of these Phase 2 results provides important support for the continued clinical development of plonmarlimab," said Dr. Isaac Meng, Chief Medical Officer of TJ Bio. "We have initiated a Phase 3 study in relapsed or refractory MAS associated with rheumatic diseases, alongside clinical development in additional indications. Through larger clinical studies, we aim to further establish the efficacy and safety of plonmarlimab and advance a potential new treatment option for patients with urgent unmet needs."

The study also included analyses of inflammatory biomarkers. Levels of ferritin and interleukin-18 (IL-18) declined markedly during treatment, and changes in IL-18 were significantly correlated with changes in ferritin. These findings suggest that IL-18 may have potential as a pharmacodynamic biomarker for assessing response to GM-CSF therapy.

"GM-CSF is a key upstream cytokine in inflammation, yet its therapeutic potential remains underexplored. Earlier development efforts largely focused on diseases driven by T cells," said Dr. Xi Chen, Chief Scientific Officer of TJ Bio. "Our pioneering work on this pathway helped demonstrate the role of GM-CSF in aberrant macrophage activation. These Phase 2 findings are consistent with our preclinical observations and strengthen the rationale for targeting GM-CSF in macrophage-driven inflammatory diseases, supporting further development of plonmarlimab across indications."

Publication details:

References:

1. Wang J, Wang R, Wang Q, et al. Plonmarlimab, a GM-CSF-neutralizing antibody, for macrophage activation syndrome. J Hematol Oncol. 2026;19:93. doi: 10.1186/s13045-026-01859-7.
2. He L, Yao S, Zhang R, et al. Macrophage activation syndrome in adults: Characteristics, outcomes, and therapeutic effectiveness of etoposide-based regimen. Front Immunol. 2022;13:955523. doi: 10.3389/fimmu.2022.955523.

About Macrophage Activation Syndrome

Macrophage activation syndrome (MAS) is a rare, life-threatening hyperinflammatory condition and a form of secondary hemophagocytic lymphohistiocytosis (sHLH). It can occur as a complication of autoimmune rheumatic diseases, including adult-onset Still's disease, systemic juvenile idiopathic arthritis and systemic lupus erythematosus. Characterized by excessive immune activation and uncontrolled systemic inflammation, MAS can lead to multiorgan dysfunction and death. Glucocorticoids and immunosuppressive therapies remain important components of treatment, but inadequate responses, relapse and treatment-related adverse effects leave substantial unmet medical needs.

About Plonmarlimab

Plonmarlimab is a high-affinity monoclonal antibody developed internally by TJ Biopharma to neutralize human granulocyte-macrophage colony-stimulating factor (GM-CSF). GM-CSF is a cytokine involved in immune regulation and inflammation. It promotes macrophage polarization toward a proinflammatory phenotype and the release of proinflammatory mediators, contributing to the development and progression of multiple autoimmune and inflammatory diseases. By specifically binding to GM-CSF, plonmarlimab blocks its interaction with its receptor and downstream signaling, with the aim of suppressing excessive immune cell activation and inflammation.

Plonmarlimab has received Breakthrough Therapy Designation from China's NMPA CDE and is being evaluated in a Phase 3 study in relapsed or refractory MAS associated with rheumatic diseases. The Company is also conducting a Phase 2 study in gouty arthritis (PRIME-2) and has received IND clearance for a Phase 2 study in sepsis (PRIME-3).

About TJ Biopharma

TJ Biopharma is a fully integrated biotech company advancing next-generation therapies in autoimmune diseases, immuno-oncology and metabolic disorders. Anchored by comprehensive R&D centers in Shanghai and Beijing and a state-of-the-art GMP manufacturing facility in Hangzhou, the Company has built a clearly differentiated two-wave pipeline. The first wave includes products that are either approved or under regulatory review, as well as other late-stage assets in registrational studies or approaching Phase 3. The second wave comprises candidates with first-in-class potential powered by the Company's proprietary Antibody^PLUS technology platforms, some of which are in Phase 1 studies while others are preparing for clinical entry. Over the years, TJ Biopharma has established a robust network of development and commercialization partnerships with Jumpcan, CSPC, Sanofi, Biogen and other leading industry players. The Company is committed to delivering innovation through a diversified and sustainable revenue model that integrates asset transactions, contract manufacturing services, and future product sales. For more information, please visit TJBio.com or follow us on LinkedIn.

TJ Biopharma Forward-Looking Statements

Certain information contained in this material may constitute "forward-looking statements" reflecting the current view of TJ Biopharma ("the Group") with respect to future events and are subject to certain risks, uncertainties and assumptions. These forward-looking statements include all matters that are not historical facts. They appear in a number of places throughout these materials and include, but are not limited to, statements regarding the Group's intentions, beliefs or current expectations concerning, among other things, results of operations, financial condition, liquidity, prospects, growth, strategies and the market. By their nature, forward-looking statements involve known and unknown risk and uncertainty because they relate to future events and circumstances. Forward-looking statements are not guarantees of future performance and the actual results of the Group's operations, financial condition and liquidity, and the development of the markets and the industry in which the Group operates may differ materially from those described in, or suggested by, the forward-looking statements contained in these materials. A number of factors could cause results and developments to differ materially from those expressed or implied by the forward-looking statements, including worldwide economic trends, the economic and political climate of the People's Republic of China, including the Hong Kong Special Administrative Region of the People's Republic of China, in particular, and changes in business strategy and various other factors. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, the actual results, performance or achievements of the Group may vary materially from those described in such forward-looking statements. The Group and its advisers undertake no obligation to update their view of such risks, uncertainties and assumptions or to release the result of any revisions to any forward-looking statements in this material that may occur due to any change in the Group's expectations or to reflect events or circumstances after the date of this material, except where they would be required to do so under applicable law.

SOURCE TJ Biopharma