DelveInsight’s “Chronic Rhinosinusitis – Pipeline Insight, 2025” reveals a strong pipeline targeting both type 2 inflammation (via IL-4/IL-13, IL-5, and TSLP blockade) and non–type 2 endotypes through novel cytokine modulators, JAK inhibitors, and epithelial barrier restoration agents. Advanced delivery approaches, including sustained-release sinus implants, high-concentration topical sprays, and drug-device combinations, are designed to maximize local efficacy while limiting systemic exposure. Late-stage candidates such as dupilumab, tezepelumab, and etokimab are showing significant improvements in polyp reduction, smell restoration, and quality-of-life scores.
With a clearer understanding of CRS endotypes and phenotypes, the 2025 development landscape is moving toward precision medicine, where treatment is matched to patient-specific inflammatory profiles. Regulatory incentives for severe, steroid-dependent CRSwNP are accelerating timelines, while microbiome-modulating therapies and anti-biofilm agents in early trials offer hope for hard-to-treat cases. As these mechanism-driven therapies advance, the coming years could redefine long-term CRS management and significantly reduce the disease’s healthcare burden.
Interested in learning more about the current treatment landscape and the key drivers shaping the Chronic Rhinosinusitis pipeline? Click here
Key Takeaways from the Chronic Rhinosinusitis Pipeline Report
• DelveInsight’s Chronic Rhinosinusitis pipeline analysis depicts a strong space with 6+ active players working to develop 6+ pipeline drugs for Chronic Rhinosinusitis treatment.
• The leading Chronic Rhinosinusitis companies include Connect Biopharma, Lyra Therapeutics, Sanotize Research and Development Corp., Regeneron Pharmaceuticals, AstraZeneca, Kyowa Kirin Co., Ltd., Keymed Biosciences Co. Ltd., Pfizer, GlycoMira Therapeutics, and others are evaluating their lead assets to improve the Chronic Rhinosinusitis treatment landscape.
• Key Chronic Rhinosinusitis pipeline therapies in various stages of development include CBP-201, LYR-210, Dupilumab, Tezepelumab, Benralizumab, CM310, PF-06817024, and others.
• In January 2025, GSK’s IL-5 inhibitor Nucala was approved in China for the treatment of individuals with inadequately controlled chronic rhinosinusitis with nasal polyps (CRSwNP), a condition affecting nearly 30 million people in the country.
• In November 2024, AstraZeneca and Amgen announced that their subcutaneous antibody Tezspire (tezepelumab) met the primary endpoint in the Phase III WAYPOINT study, showing significant efficacy in patients with chronic rhinosinusitis with nasal polyps.
• In October 2024, GSK plc announced positive Phase III results for depemokimab in adults with chronic rhinosinusitis with nasal polyps (CRSwNP). The ANCHOR-1 and ANCHOR-2 trials met their co-primary endpoints, showing significant reductions in nasal polyp score and obstruction after 52 weeks. Adverse event rates were comparable between depemokimab and placebo groups, with full results to be shared at an upcoming scientific congress.
Chronic Rhinosinusitis Overview
Chronic Rhinosinusitis (CRS) is a long-term inflammatory condition affecting the nasal passages and sinuses, lasting for 12 weeks or longer despite attempts at treatment. It is characterized by symptoms such as nasal congestion, facial pain or pressure, nasal discharge, and a reduced or lost sense of smell. CRS is typically classified into two types: CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP), each with differing pathophysiology and treatment approaches. The condition can significantly impact quality of life and is often associated with comorbidities such as asthma and allergic rhinitis.
The exact cause of CRS is multifactorial and may include infections, allergies, environmental irritants, and structural abnormalities of the nasal cavity. Treatment strategies often involve a combination of medical therapies such as nasal corticosteroids, saline irrigations, antibiotics, and biologics for severe or refractory cases. In some patients, especially those with nasal polyps or anatomical obstructions, endoscopic sinus surgery may be necessary. Newer targeted therapies, including monoclonal antibodies like dupilumab, are expanding treatment options for patients with difficult-to-treat CRS.
Find out more about Chronic Rhinosinusitis medication at https://www.delveinsight.com/report-store/chronic-rhinosinusitis-pipeline-insight
Chronic Rhinosinusitis Treatment Analysis: Drug Profile
CBP-201: Connect Biopharma
CBP-201 is a human monoclonal antibody that targets the interleukin-4 receptor alpha (IL-4Rα). It has demonstrated dose-dependent and distinct pharmacokinetic and pharmacodynamic properties in early clinical studies. Both preclinical and clinical data support that effective treatment of Th2-mediated diseases requires dual inhibition of IL-4 and IL-13. CBP-201 achieves this by binding to IL-4Rα in a way that blocks its interaction with other receptor subunits necessary for activating downstream signaling pathways. This mechanism helps address conditions such as atopic dermatitis, asthma, and nasal polyps. The therapy is currently in Phase II clinical trials for the treatment of Chronic Rhinosinusitis with Nasal Polyps (CRSwNP).
LYR-210: Lyra Therapeutics
LYR-210 is Lyra Therapeutics’ lead investigational therapy for chronic rhinosinusitis (CRS), a chronic inflammatory condition of the paranasal sinuses. It has completed Phase II clinical development. LYR-210 is a bioresorbable, implantable drug matrix developed using Lyra’s proprietary XTreo™ platform. It delivers a sustained, localized release of the corticosteroid mometasone furoate directly to the inflamed sinus tissue for up to six months from a single administration. Designed as a non-surgical alternative, LYR-210 offers a potential treatment option for CRS patients who would otherwise require sinus surgery.
Learn more about the novel and emerging Chronic Rhinosinusitis pipeline therapies.
Chronic Rhinosinusitis Therapeutics Assessment
By Product Type
• Mono
• Combination
• Mono/Combination.
By Stage
• Late-stage products (Phase III)
• Mid-stage products (Phase II)
• Early-stage product (Phase I) along with the details of
• Pre-clinical and Discovery stage candidates
• Discontinued & Inactive candidates
By Route of Administration
• Oral
• Parenteral
• Intravitreal
• Subretinal
• Topical
By Molecule Type
• Monoclonal Antibody
• Peptides
• Polymer
• Small molecule
• Gene therapy
Scope of the Chronic Rhinosinusitis Pipeline Report
• Coverage: Global
• Key Chronic Rhinosinusitis Companies: Connect Biopharma, Lyra Therapeutics, Sanotize Research and Development Corp., Regeneron Pharmaceuticals, AstraZeneca, Kyowa Kirin Co., Ltd., Keymed Biosciences Co. Ltd., Pfizer, GlycoMira Therapeutics, and others.
• Key Chronic Rhinosinusitis Pipeline Therapies: CBP-201, LYR-210, Dupilumab, Tezepelumab, Benralizumab, CM310, PF-06817024, and others.
Explore detailed insights on drugs used in the treatment of Chronic Rhinosinusitis here.
Table of Contents
1. Introduction
2. Executive Summary
3. Chronic Rhinosinusitis Pipeline: Overview
4. Analytical Perspective In-depth Commercial Assessment
5. Chronic Rhinosinusitis Pipeline Therapeutics
6. Chronic Rhinosinusitis Pipeline: Late-Stage Products (Phase III)
7. Chronic Rhinosinusitis Pipeline: Mid-Stage Products (Phase II)
8. Chronic Rhinosinusitis Pipeline: Early Stage Products (Phase I)
9. Therapeutic Assessment
10. Inactive Products
11. Company-University Collaborations (Licensing/Partnering) Analysis
12. Key Companies
13. Key Products
14. Unmet Needs
15. Market Drivers and Barriers
16. Future Perspectives and Conclusion
17. Analyst Views
18. Appendix
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