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rolvedon

Generic: eflapegrastim-xnst

rolvedon: developed by 2 companies · 1 FDA decision.

rolvedon evidence translation

What we can confirm

1 FDA record

What it means

More than one developer is source-backed. Until you choose one, AI stays drug-only and does not guess ownership.

What to watch

Watch for new trials or company disclosures after the FDA record.
BioSniper AIPage evidence connected

Prepared research question

What is verified about rolvedon, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 0 study sponsors

Related indications

Decrease the incidence of infection, as manifested by febrile neutropenia, in adult patients with nonmyeloid malignancies receiving myelosuppressive anti-cancer drugschemotherapy-induced neutropenia

Study sponsors

No additional listed-company sponsor is linked.

Development Pipeline (2)
CompanyPhase
Assertio Holdings, Inc. (ASRT)
Decrease the incidence of infection, as manifested by febril…
Approved
SPECTRUM PHARMACEUTICALS INC (SPPI)
chemotherapy-induced neutropenia
Approved
FDA Decisions1 records
BLA761148Type 1 - New Molecular EntityStandardSubcutaneousInjectable

Frequently asked questions

Who is developing rolvedon?

rolvedon is being developed by Assertio Holdings, Inc., SPECTRUM PHARMACEUTICALS INC.

What is rolvedon's latest FDA decision?

The most recent tracked FDA decision for rolvedon is Approval, dated September 9, 2022.