Drug intelligence / Profile preview

3F8 + GM-CSF + isotretinoin

Development stage
Unknown
Lead developer
Memorial Sloan Kettering Cancer Center
Modality
Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intravenous, Subcutaneous, Oral
01

Overview

This is a combination therapy used primarily for the consolidation treatment of high-risk neuroblastoma in pediatric patients who have achieved first or subsequent complete remission (CR) or very good partial remission (VGPR). The regimen consists of: - **Anti-GD2 monoclonal antibody 3F8** (murine IgG3 or its humanized form hu3F8/naxitamab), which targets the GD2 disialoganglioside antigen highly expressed on neuroblastoma cells. The antibody mediates tumor cell killing through mechanisms such as complement-dependent cytotoxicity (CDC) and especially antibody-dependent cell-mediated cytotoxicity (ADCC), engaging immune effector cells like granulocytes and monocytes. - **Granulocyte-macrophage colony-stimulating factor (GM-CSF)**, a cytokine that enhances the number and activation state of granulocytes and macrophages, thereby amplifying ADCC mediated by anti-GD2 antibodies. - **Isotretinoin** (13-cis-retinoic acid), a retinoid that induces differentiation in neuroblastoma cells to reduce minimal residual disease. The combination is designed to maximize immune-mediated clearance of residual tumor after intensive chemotherapy. Clinical studies have shown improved event-free survival when this immunotherapy is added to standard post-consolidation care[1][2][5][7][9].

Brand names
LeukineAccutane
Other names
anti-GD2 monoclonal antibody 3F8 with GM-CSF and isotretinoinanti-GD-2 monoclonal antibody 3F8 with GM-CSF and isotretinoinanti-GD 2 monoclonal antibody 3F8 with GM-CSF and isotretinoinnaxitamab (hu3F8) with GM-CSF and isotretinoin
02

Targets

CSF2R (Granulocyte-macrophage colony-stimulating factor receptor)RARA (Retinoic acid receptor alpha)GD2

Beyond the preview

Go deeper on 3F8 + GM-CSF + isotretinoin.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on 3F8 + GM-CSF + isotretinoin.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call