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Romiplostim

Aliases: Nplate

Last verified: 2026-09-23

Approved drugStrong evidencePeptidesMedium interest

The short version

A "peptibody" — a peptide TPO mimetic fused to Fc; stimulates platelet production in immune thrombocytopenia (ITP).

Identity & type

Molecular type
peptide
Origin
A "peptibody" — a peptide TPO mimetic fused to Fc; stimulates platelet production in immune thrombocytopenia (ITP).

Mechanism of action

TPO receptor (c-Mpl) agonism → megakaryocyte proliferation.

Dosing & routes

Official / clinical context

Approved drug — indications, dosing and warnings are defined by the official label. 1–10 mcg/kg SC weekly.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

1–10 mcg/kg SC weekly. Nplate: in immune thrombocytopenia raises platelets and reduces bleeding; weekly injections with platelet-level dosing.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Nplate: in immune thrombocytopenia raises platelets and reduces bleeding; weekly injections with platelet-level dosing.

Protocol — official vs community

Official / label

Nplate (immune thrombocytopenia ≥6 months, and hematopoietic acute radiation syndrome): 1 mcg/kg SC once weekly; adjust in 1 mcg/kg steps by platelet count (max 10 mcg/kg).

  1. 01Start 1 mcg/kg SC weekly
  2. 02Increase by 1 mcg/kg weekly if platelets remain <50 ×10⁹/L
  3. 03Platelets ≥200 ×10⁹/L for 2 consecutive weeks: reduce by 1 mcg/kg; >400 ×10⁹/L: hold

Duration: Chronic in ITP — platelet gains persist only while dosing continues; discontinuation planning is deliberate and tapered.

Dose-by-count weekly titration is the entire protocol; the hazard is overshoot into thrombocytosis and rebound worsening after abrupt stops. Hematology-managed biologic.

Community (anecdotal)

Structured protocol data for this entry is coming.

Human evidence

Approved 2008; also for radiation myelosuppression (H-ARS, 2021).

Preclinical evidence

The preclinical phase was completed and submitted to regulators as part of registration; pharmacology and toxicology details are part of the official label.

Known risks

  • Thromboembolism, bone-marrow fibrosis (rare), rebound thrombocytopenia.characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Real-world data outside controlled trials

Frequently asked questions

References