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NCT05641272: MM09-SLIM
Clinical Trial to Evaluate the Efficacy and Safety of Polymerized, Mannan-Conjugated Dermatophagoides Allergen Extract
Phase 2, PHASE3 trial testing 3,000 MM09 in Allergic Rhinitis in 90 participants. Not yet recruiting.
1 June 2026
Quick facts
| Lead sponsor | Inmunotek S.L. |
|---|---|
| Phase | Phase 2, PHASE3 |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | prevention |
| Enrollment | 90 |
| Start date | 1 November 2023 |
| Primary completion | 1 June 2026 |
| Estimated completion | 1 December 2026 |
| Sites | 1 location across Argentina |
Drugs / interventions tested
- 3,000 MM09 — full drug profile →
- 9,000 MM09 — full drug profile →
- Placebo sublingual
Conditions studied
- Allergic Rhinitis — all drugs for Allergic Rhinitis →
- Allergic Asthma — all drugs for Allergic Asthma →
- Allergic Rhinoconjunctivitis — all drugs for Allergic Rhinoconjunctivitis →
- Allergy to House Dust Mite — all drugs for Allergy to House Dust Mite →
Sponsor
Inmunotek S.L. — full company profile →
Who can join
Adults 12 to 60, any sex, with Allergic Rhinitis or Allergic Asthma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Prospective, randomised, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of polymerized and mannan conjugated allergen extract of Dermatophagoides for the treatment of allergic rhinitis/rhinoconjunctivitis with or without asthma. The main objective of the clinical trial is to evaluate the clinical efficacy of the investigational medicinal product, administered sublingually, compared to placebo for the treatment of moderate-severe rhinitis/rhinoconjunctivitis with or without mild to moderate asthma and controlled using the Rhinitis/Rhinoconjunctivitis Combined Symptom and Medication Score (R-CSMS).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
New progress in pediatric allergic rhinitis.
Cheng M, Dai Q, Liu Z, Wang Y, et al · · 2024 · cited 10× · PMID 39351215 · DOI 10.3389/fimmu.2024.1452410
Verify or expand the search:
- PubMed search for NCT05641272
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Inmunotek S.L. trials
Trials by the same sponsor.
- NCT07427576 — Retrospective Study Evaluating the Effectiveness and Safety of Immunotherapy With Clustoid Max Forte · completed
- NCT06790368 — Immunotherapy for the Treatment of Hymenoptera Venom Allergy in Real-life Conditions. · recruiting
- NCT06957496 — Phleum Pratense and Dactylis Glomerata Allergen Extracts Standardization · NA · completed
- NCT06782217 — Prospective Observational Study to Evaluate the Safety of Immunotherapy as a Treatment for Hymenoptera Venom Allergy · recruiting
- NCT05533385 — Juniperus Oxycedrus and Cupressus Arizonica Allergen Extracts Standardisation. · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05641272 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Inmunotek S.L.
- Last refreshed: 23 October 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05641272.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing