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Non-Hodgkin’s lymphoma (NHL) is a heterogeneous group of blood cancers originating in the lymphatic system, distinguished from Hodgkin’s lymphoma by the absence of Reed-Sternberg cells. Globally, NHL represents nearly 45% of all lymphoma cases, with a higher incidence among older adults. According to the non-Hodgkin’s lymphoma pipeline analysis by Expert Market Research, the drug pipeline encompasses monoclonal antibodies, small molecules, gene therapies, and cell-based therapies targeting both aggressive and indolent subtypes. Increasing focus on immunotherapies and targeted treatments, coupled with rising prevalence, aging populations, and unmet medical needs, is expected to drive significant growth in NHL therapeutics in the coming years.
Major companies involved in the non-Hodgkin’s lymphoma pipeline analysis include Sichuan Baili Pharmaceutical Co., Ltd., Beijing Mabworks Biotech Co., Ltd., and others.
Leading drugs currently in the pipeline include GNC-038, MBS303, N803, and others.
The pipeline shows robust growth driven by targeted therapies, including CAR-T and bispecific antibodies, alongside increasing clinical trials focusing on personalized and combination treatment approaches for improved patient outcomes.
The Non-Hodgkin’s Lymphoma Pipeline Analysis Report by Expert Market Research gives comprehensive insights into Non-Hodgkin’s lymphoma therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for non-Hodgkin’s lymphoma. The Non-Hodgkin’s lymphoma report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The Non-Hodgkin’s lymphoma pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with Non-Hodgkin’s lymphoma treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to non-Hodgkin’s lymphoma.

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Non-Hodgkin’s lymphoma is a blood cancer originating in the lymphatic system, affecting B-cells or T-cells. It develops when abnormal lymphocytes grow uncontrollably, forming tumors in lymph nodes, spleen, or other organs, often causing fatigue, swollen lymph nodes, fever, and recurrent infections.
Non-Hodgkin’s lymphoma treatments include chemotherapy, targeted therapy, immunotherapy, radiation, and stem cell transplantation to eliminate cancer cells and control disease progression. In June 2025, zanubrutinib (Brukinsa®) was approved in the UK as a treatment for relapsed or refractory mantle cell lymphoma. This oral Bruton tyrosine kinase inhibitor provides patients with an effective, convenient, home-based therapy option, reducing hospital visits.
Non-Hodgkin lymphoma (NHL) represents nearly 45% of all lymphoma cases, with the majority (85–90%) arising from B cells and the remainder from T cells or natural killer cells, as reported by Xiaobo Luo et al., 2025. In 2021, NHL contributed to approximately 962,474 disability-adjusted life years (DALYs) globally, with an age-standardized death rate (ASDR) of 13.535 per 100,000. South Asia experienced the highest regional DALYs, while Australasia reported the lowest. Eastern Sub-Saharan Africa had the highest ASDR, and High-Income North America the lowest. From 1990–2021, Southern Sub-Saharan Africa showed the largest ASDR increase, contrasted by a significant decrease in East Asia.
This section of the report covers the analysis of non-Hodgkin’s lymphoma drug candidates based on several segmentations, including:
By Phase
The pipeline assessment report covers 50+ drug analyses based on phase:
By Drug Class
The non-Hodgkin’s lymphoma pipeline analysis report covers 50+ drug analyses based on drug classes:
By Route of Administration
The pipeline assessment report covers 50+ drug analyses based on the route of administration:
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase I covers a major share of the total Non-Hodgkin’s lymphoma clinical trials, accounts for 50% of developments. It is followed by phase II at 40%. The strong focus on early and mid-phase studies indicates robust innovation, which can drive the introduction of effective therapies and positively impact market growth.
The drug molecule categories covered under the Non-Hodgkin’s lymphoma pipeline analysis include small molecules, monoclonal antibodies, peptides, and cell therapies. The Non-Hodgkin’s lymphoma report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for non-Hodgkin’s lymphoma. Targeted combination therapies are gaining attention in the non-Hodgkin’s lymphoma drug pipeline to improve treatment outcomes. For example, the ViPOR regimen, a five-drug combination including venetoclax, ibrutinib, prednisone, obinutuzumab, and lenalidomide, is under Phase Ib/II evaluation for relapsed or refractory diffuse large B-cell lymphoma. This approach targets multiple molecular pathways to enhance tumor reduction and improve patient response rates.
The EMR report for the Non-Hodgkin’s lymphoma pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed Non-Hodgkin’s lymphoma therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in non-Hodgkin’s lymphoma clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for non-Hodgkin’s lymphoma. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of non-Hodgkin’s lymphoma drug candidates.
GNC-038 is an octavalent, tetra-specific antibody being developed by Sichuan Baili Pharmaceutical Co., Ltd. for patients with relapsed or refractory non-Hodgkin’s lymphoma (NHL). The drug functions as a CD19-specific T cell engager, simultaneously targeting PD-L1 and 4-1BB to activate T cells and directly attack malignant cells. Administered via intravenous infusion once weekly, GNC-038 is currently in a Phase Ib/II study exploring its safety, tolerability, pharmacokinetics, and antitumor activity. The Phase Ib portion is determining the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D), while Phase II is assessing preliminary efficacy in NHL patients. Preclinical studies indicate strong anti-tumor activity and favorable pharmacokinetics.
MBS303 is an innovative CD20/CD3 T-cell engager being developed by Beijing Mabworks Biotech Co., Ltd. This Phase I/II study is evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of MBS303 administered via intravenous infusion in patients with relapsed or refractory B-cell non-Hodgkin’s lymphoma. MBS303 functions by redirecting T-cells to selectively target and eliminate CD20-positive B-cells, enhancing immune-mediated tumor destruction. The study is structured with a dose-escalation Phase I followed by a Phase II expansion, aiming to identify optimal dosing and preliminary therapeutic benefit. Results are expected to guide future clinical development.
CD19 t-haNK, sponsored by ImmunityBio, Inc., is undergoing a Phase 1, first-in-human study to evaluate its safety as a single agent and in combination with rituximab, with or without the IL-15 superagonist N-803, in subjects with relapsed or refractory Non-Hodgkin’s Lymphoma (R/R NHL). This open-label study is examining the drug’s safety, tolerability, and preliminary efficacy through intravenous administration following lymphodepleting chemotherapy. CD19 t-haNK is an engineered natural killer cell therapy targeting CD19-positive B cells, while N-803 stimulates proliferation of NK and T cells, enhancing the immune response. Up to 20 subjects are being enrolled to assess safety and preliminary efficacy.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Non-Hodgkin’s Lymphoma Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for non-Hodgkin’s lymphoma. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into Non-Hodgkin’s lymphoma collaborations, regulatory environments, and potential growth opportunities.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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