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Grafalon

St. Anna Kinderkrebsforschung · FDA-approved active Small molecule ✓ Verified May 2026

Grafalon is a Small molecule drug developed by St. Anna Kinderkrebsforschung. It is currently FDA-approved. Also known as: Anti-human T-lymphocyte immunoglobulin.

Grafalon is a medication used to treat various conditions, including Renal Transplantation, Graft Vs Host Disease, Peripheral Blood Stem Cell Transplantation, Acute Myeloid Leukemia (AML), and Myelodysplastic Syndromes (MDS). It is administered as an anti-lymphocyte globulin, typically given at doses of 0.5 mg/kg/day, 1 mg/kg/day, or 2 mg/kg/day for 5 consecutive days.

At a glance

Generic nameGrafalon
Also known asAnti-human T-lymphocyte immunoglobulin
SponsorSt. Anna Kinderkrebsforschung
ModalitySmall molecule
Therapeutic areaOther
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 Grafalon

What is Grafalon?

Grafalon is a Small molecule drug developed by St. Anna Kinderkrebsforschung.

Who makes Grafalon?

Grafalon is developed and marketed by St. Anna Kinderkrebsforschung (see full St. Anna Kinderkrebsforschung pipeline at /company/st-anna-kinderkrebsforschung).

Is Grafalon also known as anything else?

Grafalon is also known as Anti-human T-lymphocyte immunoglobulin.

What development phase is Grafalon in?

Grafalon is FDA-approved (marketed).

Related

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