Elinzanetant
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| Trade names | Lynkuet |
| Other names | BAY-3427080; GSK-1144814; GSK-1144814A; NT-814 |
| AHFS/Drugs.com | Multum Consumer Information |
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| Routes of administration | Oral[1] |
| Drug class | Neurokinin NK1 and NK3 receptor antagonist |
| ATC code | |
| Legal status | |
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| CAS Number | |
| PubChem CID | |
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| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C33H35F7N4O3 |
| Molar mass | 668.657 g·mol−1 |
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Elinzanetant, sold under the brand name Lynkuet, is a medication used for the treatment of moderate to severe vasomotor symptoms (hot flashes) due to menopause.[1] It is taken orally.[1]
The drug acts as a selective neurokinin NK1 and NK3 receptor antagonist.[1][5]
Medical uses
Elinzanetant is indicated for the treatment of moderate to severe vasomotor symptoms associated with menopause.[1]
Pharmacology
Pharmacodynamics
Elinzanetant has been found to dose-dependently suppress luteinizing hormone, estradiol, and progesterone levels in premenopausal women.[7][8]
History
Elinzanetant was developed by Bayer Healthcare.[1]
In September 2025, the Committee for Medicinal Products for Human Use of the European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Lynkuet, intended for the treatment of moderate to severe vasomotor symptoms (hot flushes).[5] The applicant for this medicinal product is Bayer AG.[5] Elinzanetant was authorized for medical use in the European Union in November 2025.[5][6]
Lynkuet was approved for medical use in the United States in October 2025.[9][10]
Society and culture
Names
Elinzanetant is the International Nonproprietary Name (INN).[11]
Elinzanetant is sold under the brand name Lynkuet.[12]
Research
In addition to approval for vasomotor symptoms, elinzanetant is under development for the treatment of sleep disorders.[13] It is in phase 2 clinical trials for this indication.[13] The drug was also under development for the treatment of schizophrenia and opioid-related disorders, but development was discontinued for these uses.[13]
References
- ^ a b c d e f g "Lynkuet- elinzanetant capsule". DailyMed. 28 October 2025. Retrieved 24 December 2025.
- ^ "Details for: Lynkuet". Drug and Health Products Portal. 23 July 2025. Retrieved 28 September 2025.
- ^ "Lynkuet product information". Lynkuet. 23 July 2025. Retrieved 28 September 2025.
- ^ "MHRA approves elinzanetant to treat moderate to severe vasomotor symptoms (hot flushes) caused by menopause". Medicines and Healthcare products Regulatory Agency (Press release). 8 July 2025. Retrieved 28 September 2025.
- ^ a b c d e "Lynkuet EPAR". European Medicines Agency (EMA). 19 September 2025. Retrieved 27 September 2025. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ a b "Lynkuet PI". Union Register of medicinal products. 18 November 2025. Retrieved 1 December 2025.
- ^ Depypere H, Lademacher C, Siddiqui E, Fraser GL (July 2021). "Fezolinetant in the treatment of vasomotor symptoms associated with menopause". Expert Opin Investig Drugs. 30 (7): 681–694. doi:10.1080/13543784.2021.1893305. PMID 33724119.
- ^ Pawsey S, Mills EG, Ballantyne E, Donaldson K, Kerr M, Trower M, et al. (July 2021). "Elinzanetant (NT-814), a Neurokinin 1,3 Receptor Antagonist, Reduces Estradiol and Progesterone in Healthy Women". The Journal of Clinical Endocrinology and Metabolism. 106 (8): e3221–e3234. doi:10.1210/clinem/dgab108. PMC 8277204. PMID 33624806.
- ^ "Novel Drug Approvals for 2025". U.S. Food and Drug Administration (FDA). 24 October 2025. Retrieved 29 October 2025.
- ^ Lee A (November 2025). "Elinzanetant: First Approval". Drugs. doi:10.1007/s40265-025-02244-3. PMID 41222830.
- ^ World Health Organization (2020). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 84". WHO Drug Information. 34 (3). hdl:10665/340680.
- ^ "Bayer's Lynkuet (elinzanetant), the First and Only Neurokinin 1 and Neurokinin 3 Receptor Antagonist, Receives FDA Approval for Moderate to Severe Hot Flashes Due to Menopause" (Press release). Bayer. 24 October 2025. Retrieved 29 October 2025 – via Business Wire.
- ^ a b c "Elinzanetant". AdisInsight. 24 November 2025. Retrieved 13 January 2026.
External links
- Clinical trial number NCT05042362 for "A Study to Learn More About How Well Elinzanetant Works and How Safe it is for the Treatment of Vasomotor Symptoms (Hot Flashes) That Are Caused by Hormonal Changes Over 26 Weeks in Women Who Have Been Through the Menopause (OASIS-1)" at ClinicalTrials.gov
- Clinical trial number NCT05099159 for "A Study to Learn More About How Well Elinzanetant Works and How Safe it is for the Treatment of Vasomotor Symptoms (Hot Flashes) That Are Caused by Hormonal Changes Over 26 Weeks in Women Who Have Been Through the Menopause (OASIS-2)" at ClinicalTrials.gov