Ph1b/2 Study of the Safety and Efficacy of T-DXd Combinations in Advanced HER2-expressing Gastric Cancer (DESTINY-Gastric03)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-130
SponsorAstraZeneca

About this trial

DESTINY-Gastric03 will investigate the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of trastuzumab deruxtecan (T-DXd) alone or in combination with chemotherapy and/or immunotherapy in HER2-expressing advanced/metastatic gastric/gastroesophageal junction (GEJ) and esophageal adenocarcinoma patients.

Study hypotheses: Combination of T-DXd with cytotoxic chemotherapy and/or immunotherapy administered to subjects at the recommended phase 2 dose will show manageable safety and tolerability and preliminary anti-tumor efficacy so as to permit further clinical testing. T-DXd in combination with cytotoxic chemotherapy or immune checkpoint inhibitor administered to HER2-expressing gastric, GEJ and esophageal cancer patients who have not received prior treatment for advanced/metastatic disease will show preliminary evidence of anti-tumour activity and the potential to become a therapeutic option for this patient population.

Eligibility criteria

Qualifiers

Male and female participants must be at least 18 years of age. Other age restrictions may apply as per local regulations

Locally advanced, unresectable, or metastatic disease based on most recent imaging

For Part 1, 2, 3a, 4a pathologically documented adenocarcinoma of the stomach/GEJ/esophagus, HER2-positive (IHC 3+ or IHC 2+/ISH+) based on local tissue testing results

For Part 3b,4b and Part 5, pathologically documented adenocarcinoma of the stomach/GEJ/esophagus, HER2-low (IHC 2+/ISH-negative or IHC 1+) based on local tissue testing results

Disqualifiers

Part 1 to 4: History of active primary immunodeficiency, known HIV, active chronic, or past hepatitis B infection, or hepatitis C infection. Part 5: evidence of active, uncontroled HIV, HBV or HCV infection.

Uncontrolled intercurrent illness.

History of non-infectious pneumonitis/ILD, current ILD, or where suspected ILD that cannot be ruled out by imaging at screening.

Lung-specific intercurrent clinically significant severe illnesses.

Trial design

Treatments tested in this trial

  • Fluorouracil (5-FU)
  • Capecitabine
  • Durvalumab
  • Oxaliplatin
  • Trastuzumab
  • Trastuzumab deruxtecan
  • Cisplatin
  • Pembrolizumab
  • Volrustomig
  • Rilvegostomig

Treatment groups

450 Participants
are divided into 18 treatment groups

18

Treatment groups

See each treatment group below.

Locations

100
Brazil
Research Site88020-210, Florianópolis Brazil
Research Site86015-520, Londrina Brazil
Research Site59075-740, Natal Brazil
Research Site90160-093, Porto Alegre Brazil

Sponsors and collaborators

AstraZeneca

Lead sponsor

Daiichi Sankyo

Collaborator