Drug intelligence / Profile preview

R-DHAOx

Development stage
Unknown
Modality
Vaccines & Immunotherapeutics, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

R-DHAOx is a combination chemotherapy regimen used primarily for treating relapsed or refractory B-cell non-Hodgkin lymphoma. The regimen consists of four medications: rituximab, dexamethasone, high-dose cytarabine (Ara-C), and oxaliplatin. ## Composition and Administration R-DHAOx is typically administered as follows: - Rituximab: 375 mg/m² intravenously on day 1 - Dexamethasone: 40 mg daily on days 1-4 - Cytarabine (Ara-C): 2,000 mg/m² twice daily on day 2 - Oxaliplatin: 100 mg/m² intravenously on day 1 The treatment cycle is repeated every 21 days, with the number of cycles determined by the patient's response and tolerance[1][3]. ## Efficacy and Applications This regimen has shown significant efficacy in treating various types of B-cell non-Hodgkin lymphomas, including: - Diffuse large B-cell lymphoma (DLBCL) - Follicular lymphoma (FL) - Mantle cell lymphoma - Marginal zone lymphoma[3][6] In clinical studies, R-DHAOx has demonstrated impressive response rates: - Overall response rates of 71-75% - Complete response rates of 57-68% - Two-year overall survival rates of approximately 75%[3][6] ## Development and Rationale R-DHAOx was developed as a modification of the R-DHAP regimen (rituximab, dexamethasone, high-dose cytarabine, and cisplatin). The key difference is the substitution of oxaliplatin for cisplatin to reduce nephrotoxicity while maintaining efficacy[8]. ## Toxicity Profile The most common adverse effects include: - Hematological toxicities: neutropenia (44%), thrombocytopenia (47%), and anemia - Neurological toxicities: primarily transient sensory or motor neuropathies - Cold sensitivity: patients are advised to avoid cold drinks, food, and ice during treatment and for up to 2 days after oxaliplatin administration[3][5] Importantly, R-DHAOx shows significantly less nephrotoxicity compared to cisplatin-containing regimens, making it suitable for patients with renal impairment[8]. ## Current Applications R-DHAOx is primarily used as: 1. Salvage therapy for relapsed/refractory B-cell non-Hodgkin lymphomas 2. A bridge to autologous stem cell transplantation in eligible patients 3. Part of combination approaches with newer agents like BTK inhibitors (e.g., zanubrutinib)[7] The regimen has shown efficacy across different age groups, though dose adjustments may be considered for patients over 60 years of age[1].

Other names
DHAXR-DHAXDHAX-R regimen
02

Targets

GR (Glucocorticoid receptor)CD20 (B-lymphocyte antigen CD20)DNA

Beyond the preview

Go deeper on R-DHAOx.

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 R-DHAOx.

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