Enhertu (fam-trastuzumab deruxtecan-nxki) vs Jeselhy (pimitespib) ()

Enhertu (fam-trastuzumab deruxtecan-nxki) vs Jeselhy (pimitespib) ()

Enhertu (fam-trastuzumab deruxtecan-nxki) is an antibody-drug conjugate specifically approved for the treatment of certain types of breast cancer and gastric cancer that overexpress HER2, a protein that promotes the growth of cancer cells. Jeselhy (pimitespib), on the other hand, is a heat shock protein 90 (HSP90) inhibitor, which is a type of targeted therapy that interferes with the function of multiple proteins involved in cancer cell growth and survival, and as of my knowledge cutoff date, it is not approved for use. When deciding between these two medications, it is crucial to consider the specific type of cancer, its molecular characteristics, and the approval status of the medication, as well as consulting with a healthcare professional who can provide personalized medical advice based on the patient's unique medical history and condition.

Difference between Enhertu and Jeselhy (pimitespib)

Metric Enhertu (fam-trastuzumab deruxtecan-nxki) Jeselhy (pimitespib)
Generic name Fam-trastuzumab deruxtecan-nxki Pimitespib
Indications HER2-positive breast cancer, HER2-positive gastric or gastroesophageal junction adenocarcinoma Currently under investigation, not yet approved
Mechanism of action Antibody-drug conjugate targeting HER2 receptors HSP90 inhibitor
Brand names Enhertu Jeselhy (tentative, as drug is not yet approved)
Administrative route IV infusion Not available
Side effects Nausea, fatigue, vomiting, alopecia, constipation, decreased appetite, anemia, neutropenia, etc. Not available
Contraindications History of interstitial lung disease, pneumonitis, severe hypersensitivity to trastuzumab deruxtecan Not available
Drug class Antibody-drug conjugate HSP90 inhibitor
Manufacturer Daiichi Sankyo and AstraZeneca Taiho Pharmaceutical

Efficacy

Enhertu (fam-trastuzumab deruxtecan-nxki) for Gastric Cancer

Enhertu (fam-trastuzumab deruxtecan-nxki) is an antibody-drug conjugate that has shown efficacy in the treatment of HER2-positive gastric or gastroesophageal junction (GEJ) cancer. It is specifically designed to target and deliver chemotherapy directly to cancer cells that overexpress HER2, a protein that can promote the growth of cancer cells. In clinical trials, Enhertu has demonstrated significant improvements in overall survival and progression-free survival compared to standard treatments. For instance, the pivotal Phase 2 trial, DESTINY-Gastric01, showed that patients treated with Enhertu had a median overall survival of 12.5 months compared to 8.4 months for those treated with chemotherapy alone.

The efficacy of Enhertu in gastric cancer was further supported by the results of the Phase 3 DESTINY-Gastric02 trial, which confirmed the survival benefit and showed a higher objective response rate in patients receiving Enhertu. The drug has received approval in several countries for use in patients with unresectable or metastatic HER2-positive gastric or GEJ cancer who have previously received a trastuzumab-based regimen. This approval marks a significant advancement in the treatment options available for this aggressive form of cancer.

Jeselhy (pimitespib) for Gastric Cancer

Jeselhy (pimitespib) is a novel therapeutic agent under investigation for the treatment of gastric cancer. It is a heat shock protein 90 (HSP90) inhibitor, which plays a role in the stabilization and proper function of various proteins that are essential for the growth and survival of cancer cells. By inhibiting HSP90, Jeselhy aims to disrupt these processes and exert antitumor effects. While Jeselhy is still in the clinical development stages, early trial results have shown promise in the treatment of advanced gastric cancer, particularly in patients who have exhausted other treatment options.

For example, in early-phase clinical studies, Jeselhy has demonstrated a manageable safety profile and preliminary signs of efficacy in patients with gastric cancer. The ongoing research is focused on determining the optimal dosing, understanding the spectrum of its activity against various gastric cancer subtypes, and evaluating its efficacy in combination with other therapies. As of the current knowledge cutoff, Jeselhy continues to be studied, and further results from clinical trials are awaited to establish its potential role in the treatment landscape of gastric cancer.

Regulatory Agency Approvals

Enhertu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Jeselhy (pimitespib)
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Enhertu or Jeselhy (pimitespib) today

If Enhertu or Jeselhy (pimitespib) are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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