Follicular Lymphoma Clinical Trial Pipeline Accelerates as 45+ Pharma Companies Rigorously Develop Drugs for Market Entry | DelveInsight

DelveInsight's, "Follicular Lymphoma Pipeline Insight, 2025" report provides comprehensive insights about 45+ companies and 50+ pipeline drugs in Follicular Lymphoma pipeline landscape. It covers the Follicular Lymphoma pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Follicular Lymphoma pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

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Key Takeaways from the Follicular Lymphoma Pipeline Report

* On January 20, 2026- AstraZeneca announced a Phase III, multicentre, open-label study evaluating the efficacy, safety and the degree of added benefit of the Surovatamig (AZD0486) plus rituximab combination compared to Investigator's choice of 3 standard immunochemotherapy regimen, conducted in participants with untreated FL.
* On January 12, 2026- BeiGene conducted a study is to compare the efficacy of zanubrutinib plus obinutuzumab versus lenalidomide plus rituximab (R^2) in participants with relapsed/refractory (R/R) follicular lymphoma (FL), as measured by progression-free survival as determined by an independent review committee in accordance with the 2014 modification of the International Working Group on non-Hodgkin lymphoma (NHL) Criteria based on n positron emission tomography and computed tomography (PET/CT), and to compare the efficacy of zanubrutinib plus rituximab versus R^2 in participants with R/R marginal zone lymphoma (MZL), as measured by progression free survival (PFS) assessed by IRC in accordance with CT-based Lugano 2014 Criteria.
* On January 09, 2026- Genmab conducted a trial is to identify the most appropriate dose of epcoritamab, and the aim of the second part of the trial is to assess the selected epcoritamab dose in a larger group of participants with B-NHL. All participants in this trial will receive either epcoritamab alone, or epcoritamab combined with another standard treatment regimen, with a total of 10 different treatment
* On January 09, 2026- Regeneron Pharmaceuticals conducted a study is researching an experimental drug called odronextamab (referred to as study drug), in combination with lenalidomide. The study is focused on participants who have one of two types of cancer: follicular lymphoma (FL) or marginal zone lymphoma (MZL) that has come back after treatment (called "relapsed"), or did not respond to treatment (called "refractory"). FL and MZL are subtypes of Non-Hodgkin 's lymphoma (NHL).
* On January 09, 2026- Hoffmann-La Roche initiated a study will evaluate the efficacy and safety of mosunetuzumab in combination with lenalidomide (M + Len) compared to rituximab in combination with lenalidomide (R + Len) in participants with relapsed or refractory (R/R) follicular lymphoma (FL) who have received at least one line of prior systemic therapy.
* On January 08, 2026- Celgene announced a Phase 2 Randomized, Open Label Study to Evaluate the Efficacy and Safety of Golcadomide in Combination With Rituximab in Participants With Newly Diagnosed Advanced Stage Follicular Lymphoma
* DelveInsight's Follicular Lymphoma Pipeline analysis depicts a robust space with 45+ Follicular Lymphoma companies working to develop 50+ pipeline treatment therapies.
* The leading Follicular Lymphoma Companies such as Mab Works, AstraZeneca, ADC Therapeutics, Xynomic Pharmaceuticals, AbbVie, Nurix, InnoCare Pharma, LTZ Therapeutics, Hutchmed, Regeneron Pharmaceuticals, Pfizer, InnoCare Pharma, TriSalus Life Sciences, BeiGene and others.
* Promising Follicular Lymphoma Pipeline Therapies such as DRL_RI (Proposed rituximab biosimilar), MabThera Registered , Epcoritamab, Rituximab, Lenalidomide, and others.

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The Follicular Lymphoma Pipeline Report provides a disease overview, pipeline scenario, and therapeutic assessment of the key pipeline therapies in this domain. The Follicular Lymphoma Pipeline Report also highlights the unmet needs with respect to the Follicular Lymphoma.

Follicular Lymphoma Overview

Follicular lymphoma (FL) is a slow-growing type of non-Hodgkin lymphoma (NHL) that arises from B lymphocytes, a type of white blood cell integral to the immune system. It is characterized by the formation of abnormal lymphoid follicles in lymph nodes and other lymphatic tissues. Accounting for about 20% of all NHL cases, FL typically presents with painless lymphadenopathy, often accompanied by symptoms like fatigue, night sweats, or unintentional weight loss in advanced stages. While generally considered indolent, FL can transform into a more aggressive form of lymphoma, necessitating vigilant monitoring. Advances in treatment, including immunotherapy and targeted therapies, have significantly improved outcomes for patients with this condition.

Follicular Lymphoma Emerging Drugs

* MIL62: MAB WORKS

MIL62 is a third-generation anti-CD20 antibody with a unique competitive position. MIL62 is the first domestically developed third-generation anti-CD20 antibody entering Phase III registration trial in China. MIL62 is self-developed by leveraging our ADCC-enhanced antibody platform. In in vitro and in vivo studies, MIL62 demonstrates stronger ADCC and anti-tumor activities than rituximab (first-generation anti-CD20 antibodies) and obinutuzumab (other third-generation anti-CD20 antibody). The company is implementing critical clinical development strategies to first pursue marketing approval from the NMPA for the treatment of relapsed and/or refractory FL patients and DLBCL patients. At the same time, MIL62 is being developed for previously untreated FL and DLBCL patients (a significantly larger patient population) by demonstrating clinical superiority over rituximab. Currently the drug is in Phase III stage of its development for the treatment of follicular lymphoma.

* AZD0486: AstraZeneca

AZD0486, also known as TNB-486, is an innovative bispecific antibody targeting CD19 and CD3, designed to enhance T-cell-mediated destruction of malignant B cells, particularly in patients with relapsed or refractory follicular lymphoma (FL). AZD0486 functions by engaging T-cells to attack B-cell malignancies, thereby circumventing some limitations associated with traditional therapies. Its design incorporates a low-affinity anti-CD3 moiety, which helps mitigate severe cytokine release syndrome (CRS), a common side effect of T-cell engagers. This unique feature allows for a more controlled immune response, potentially leading to better safety profiles. Currently, the drug is in Phase III stage of its clinical trial for the treatment of Follicular Lymphoma.

* Abexinostat: Xynomic Pharmaceuticals

Abexinostat (Abx) is a novel, potent, orally administered pan-histone deacetylase inhibitor (HDACi) developed by Xynomic Pharmaceuticals. It is designed to maintain effective anti-tumor concentrations through twice-daily (BID) dosing. Abexinostat targets multiple HDAC enzymes, which are involved in the deacetylation of histones, leading to chromatin remodeling and regulation of gene expression. By inhibiting HDACs, Abexinostat causes the accumulation of acetylated histones, promoting apoptosis, cell cycle arrest, and inhibition of angiogenesis in cancer cells. Additionally, Abexinostat acts as a Rad51 recombinase inhibitor, interfering with DNA repair mechanisms, which enhances its anti-cancer activity. Currently, the drug is in Phase II stage of its clinical trial for the treatment of Follicular Lymphoma.

* ABBV-319: AbbVie

ABBV-319 is a CD19-targeting antibody-drug conjugate engineered to reduce glucocorticoid-associated toxicities while possessing 3 distinct mechanisms of action (MOA) to increase therapeutic efficacy: (1) antibody-mediated delivery of a glucocorticoid receptor modulator (GRM) payload to activate apoptosis, (2) inhibition of CD19 signaling, and (3) enhanced fragment crystallizable (Fc)-mediated effector function via afucosylation of the antibody backbone. Currently, the drug is in the Phase I stage of development to treat Follicular Lymphoma.

* NX-2127: Nurix Therapeutics, Inc.

NX-2127 is an oral small molecule degrader of BTK and cereblon neosubstrates IKZF1 (Ikaros) and IKZF3 (Aiolos). Cereblon immunomodulatory drugs that induce degradation IKZF1 and IKZF3 such as lenalidomide and pomalidomide are FDA approved for a variety of hematologic malignancies including multiple myeloma, follicular lymphoma, and mantle cell lymphoma. We hypothesize that the combination of BTK degradation and cereblon immunomodulatory activity will have enhanced therapeutic benefit in patients suffering from a variety of B-cell malignancies. Initial clinical data support the activity of NX-2127 in patients whose tumors harbor either wild-type BTK or BTK with mutations conferring clinical resistance to FDA approved agents. Initial clinical data also confirm potent BTK degradation with once daily oral dosing. Currently, the drug is in the Phase I stage of its development for the treatment of Follicular Lymphoma.

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The Follicular Lymphoma pipeline report provides insights into

* The report provides detailed insights about companies that are developing therapies for the treatment of Follicular Lymphoma with aggregate therapies developed by each company for the same.
* It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Follicular Lymphoma Treatment.
* Follicular Lymphoma Companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
* Follicular Lymphoma Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type.
* Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Follicular Lymphoma market.

Follicular Lymphoma Companies

Mab Works, AstraZeneca, ADC Therapeutics, Xynomic Pharmaceuticals, AbbVie, Nurix, InnoCare Pharma, LTZ Therapeutics, Hutchmed, Regeneron Pharmaceuticals, Pfizer, InnoCare Pharma, TriSalus Life Sciences, BeiGene and others.

Follicular Lymphoma pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

* Oral
* Intravenous
* Subcutaneous
* Parenteral
* Topical

Follicular Lymphoma Products have been categorized under various Molecule types such as

* Recombinant fusion proteins
* Small molecule
* Monoclonal antibody
* Peptide
* Polymer
* Gene therapy

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Scope of the Follicular Lymphoma Pipeline Report

* Coverage- Global
* Follicular Lymphoma Companies- Mab Works, AstraZeneca, ADC Therapeutics, Xynomic Pharmaceuticals, AbbVie, Nurix, InnoCare Pharma, LTZ Therapeutics, Hutchmed, Regeneron Pharmaceuticals, Pfizer, InnoCare Pharma, TriSalus Life Sciences, BeiGene and others.
* Follicular Lymphoma Pipeline Therapies- DRL_RI (Proposed rituximab biosimilar), MabThera Registered , Epcoritamab, Rituximab, Lenalidomide, and others.
* Follicular Lymphoma Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
* Follicular Lymphoma Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III

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Table of Contents

* Introduction
* Executive Summary
* Follicular Lymphoma: Overview
* Pipeline Therapeutics
* Therapeutic Assessment
* Follicular Lymphoma- DelveInsight's Analytical Perspective
* Late Stage Products (Phase III)
* MIL62: MAB WORKS
* Mid Stage Products (Phase II)
* Abexinostat: Xynomic Pharmaceuticals
* Early Stage Products (Phase I)
* ABBV-319: AbbVie
* Preclinical and Discovery Stage Products
* Drug name: Company name
* Inactive Products
* Follicular Lymphoma Key Companies
* Follicular Lymphoma Key Products
* Follicular Lymphoma- Unmet Needs
* Follicular Lymphoma- Market Drivers and Barriers
* Follicular Lymphoma- Future Perspectives and Conclusion
* Follicular Lymphoma Analyst Views
* Follicular Lymphoma Key Companies
* Appendix

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