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Novel delivery platforms for OTC allergic rhinitis relief
  • Background
  • What we're looking for
  • What we can offer you
  • Who we are
  • Q&A
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Get them answered by the team at Haleon.
Background

Allergic rhinitis—triggered by airborne irritants such as pollen, dust mites, mold, and pet dander—causes congestion, sneezing, rhinorrhea, and ocular itching that disrupt sleep and productivity. Current over-the-counter options (oral antihistamines, decongestants, intranasal sprays) can be slow to act, sedating, or difficult to use consistently, leading to poor adherence and sub-optimal control. Advances in drug formulation, digital health, and materials science create an opportunity to reinvent consumer-friendly therapies that combine rapid, durable efficacy with personalized guidance, minimal side effects, and environmentally responsible design.

What we're looking for

We are looking for technology-driven OTC solutions that deliver rapid, sustained relief from allergic rhinitis while improving user adherence, safety, and overall experience.

Solutions of interest include:
  • Muco-adhesive nasal mists or gels
  • Rapid-dissolving oral films/tablets with non-sedating antihistamines
  • Skin or nasal micro-patches enabling timed trans-mucosal delivery
  • Dry-powder or soft-mist inhalers targeting the upper airway only
  • Drug-free barrier sprays or nasal filters with proven allergen blocking
  • AI-enabled mobile apps for symptom tracking & dose reminders
  • Wearable or IoT sensors that link pollen counts to adaptive dosing
  • Modular platforms that allow easy add-on of new actives or data services
  • Portable vibrating-mesh nebulizers for targeted nasal deposition
Our must-have requirements are:
  • Clinically supported onset of action ≤15 min and duration ≥8 hr
  • Demonstrated or strongly reasoned safety profile for adolescent (13+) and adult use
  • User-friendly design enabling accurate self-administration in ≤3 steps
Our nice-to-have's are:
  • Manufacturable at a commercial scale
  • Non-drowsy
  • Refillable, propellant-free devices using plant-based or PCR plastics
  • Demonstrated or strongly reasoned pediatric safety
What's out of scope:
  • Prescription-only biologics or allergen immunotherapy regimens
  • Systemic corticosteroid products requiring medical supervision
  • Invasive implantable or surgically placed devices
  • Solutions dependent on cold-chain distribution or single-use propellants
  • Complex medical devices that are difficult to use at home
  • Technologies requiring health care provider supervision
Acceptable technology readiness levels (TRL):
Levels 4-9
What we can offer you
Eligible partnership models:
Sponsored researchLicensingSupply/purchaseCo-development
Benefits:
Sponsored Research
Funding is proposal-dependent, starting with a proof-of-concept project that has the potential for expansion based on results and opportunities. The funding range is typically from $25,000 to $100,000 for a six-month project.
Expertise
We also offer the expertise of our team of scientists for collaboration and guidance during the project’s development. Possible partnerships with us include, but are not limited to, sponsored research, joint development, supply, consulting, and licensing.
Who we are

Our global team is dedicated to developing and collaborating on future-facing, scientifically proven, consumer-focused innovations and technologies. We believe that true innovation comes from collaboration and partnerships with start-ups, academia, health tech pioneers, and innovators.

Haleon has a strong portfolio of consumer health brands and plays a vital role for people all around the world, in a sector that is growing and more relevant than ever. We have five brand categories: Oral Health, Vitamins, Minerals and Supplements(VMS), Pain, Respiratory & Digestive. Our trusted brands like Sensodyne, Advil, Centrum & Voltaren improve the lives of millions globally.

 Learn more
Reviewers
Q&A with Haleon

The Q&A is now closed.

Sort by:
Q.
Whether early-stage applications (e.g., IND or exploratory partnerships) require preliminary human data to justify the proposed onset/duration and safety profile?
2
A.
Dear Guochen, Thank you for your question. We are open to explore early-stage proposals supported by validation in lab setting. Any preliminary data on human would be more than welcome to justify specific onset/safety profile, but are not required. I would recommend going ahead and submitting your proposal with the preliminary details you have produced. We will review all entries together with our experts. Thanks again for your interest—we’re looking forward to learning more about your idea!
MG
Matteo Gasbarri, External Innovation Senior Scientist, Haleon
June 18, 2025
Is this response helpful?
0
0
Q.
Our team is developing a novel CBD-based nasal rinse to treat chronic rhinosinusitis (CRS) using its targeted anti-inflammatory properties, mediated by the endocannabinoid system. Promising results in murine models show significant reductions in eosinophilic inflammatory markers. We believe our CBD nasal rinse’s fundamental anti-inflammatory mechanism and local delivery system could be applicable to other sinonasal inflammatory conditions, including allergic rhinitis. Does an innovation targeting broader sinonasal inflammation, with potential for OTC development and a novel mechanism like ours, would be eligible within this RFS scope?
1
A.
Dear Mehdi, Thank you for your comment, and we really appreciate your interest in submitting a proposal for this brief. We would be very keen to assess such solution, targeting broader sino-nasal inflammation, based on CBD. I would recommend going ahead and submitting your proposal with preliminary details about your project. Once the submission period closes, we will review all entries together with our experts. Thanks again for your interest—we’re looking forward to learning more about your idea!
MG
Matteo Gasbarri, External Innovation Senior Scientist, Haleon
June 18, 2025
Is this response helpful?
0
0
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