Last reviewed · How we verify

Luveris® 25 IU

EMD Serono · FDA-approved active Small molecule ✓ Verified May 2026 Quality 2/100

Luveris® 25 IU is a Small molecule drug developed by EMD Serono. It is currently FDA-approved. Also known as: Lutropin alfa, Recombinant human luteinizing hormone (r-hLH).

Luveris 25 IU is a medication used to treat Hypogonadotropic Hypogonadism and Infertility in women. It is a form of Lutropin Alfa for Injection, which stimulates the production of luteinizing hormone (LH) in the body.

At a glance

Generic nameLuveris® 25 IU
Also known asLutropin alfa, Recombinant human luteinizing hormone (r-hLH)
SponsorEMD Serono
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Luveris® 25 IU

What is Luveris® 25 IU?

Luveris® 25 IU is a Small molecule drug developed by EMD Serono.

Who makes Luveris® 25 IU?

Luveris® 25 IU is developed and marketed by EMD Serono (see full EMD Serono pipeline at /company/emd-serono).

Is Luveris® 25 IU also known as anything else?

Luveris® 25 IU is also known as Lutropin alfa, Recombinant human luteinizing hormone (r-hLH).

What development phase is Luveris® 25 IU in?

Luveris® 25 IU is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing