Drug intelligence / Profile preview

S-1 + oxaliplatin + olaparib

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

The combination of S-1, oxaliplatin, and olaparib represents a therapeutic approach that combines different mechanisms of action to target cancer cells. This combination includes a fluoropyrimidine antimetabolite (S-1), a platinum-based chemotherapy agent (oxaliplatin), and a PARP inhibitor (olaparib). ## Mechanism of Action This combination works through multiple pathways: 1. **Oxaliplatin** is a platinum-based chemotherapy agent that causes DNA damage through DNA crosslinking, particularly intrastrand and interstrand crosslinking[5]. It's commonly used to treat colorectal cancer and is typically administered in combination with fluorouracil and leucovorin (FOLFOX regimen)[5]. 2. **Olaparib** is a PARP (Poly ADP-ribose polymerase) inhibitor that blocks DNA repair mechanisms. Studies show that olaparib can increase the sensitivity of cancer cells to oxaliplatin by enhancing induced DNA double-strand breaks[2][3]. The combination of olaparib and oxaliplatin significantly increases cytotoxic effects compared to either agent alone[1][2]. 3. **S-1** is an oral fluoropyrimidine that combines tegafur (a prodrug of 5-fluorouracil) with two modulators. It's mentioned in the context of combination chemotherapy for advanced gastric cancer[1]. ## Research Findings Research has demonstrated that: - The combination of olaparib and oxaliplatin significantly reduces cell survival compared to oxaliplatin alone[1]. - This combination inhibits tumor cell proliferation by inducing cell cycle arrest and apoptosis, particularly in XRCC2-deficient colorectal cancer cells[2]. - The combined treatment increases DNA damage markers (γH2AX) compared to either drug alone[1][2][3]. - Olaparib changes the expression of PARP1 and enhances the sensitivity of cancer cells to oxaliplatin[1]. - The combination effectively inhibits the viability, size, cell count, and proliferation of organoids derived from oxaliplatin-resistant gastric cancers[3]. This triple combination represents a promising approach for treating various cancers, particularly those that have developed resistance to standard treatments.

02

Targets

DNATS (Thymidylate synthase)

Beyond the preview

Go deeper on S-1 + oxaliplatin + olaparib.

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 S-1 + oxaliplatin + olaparib.

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