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Phase 2 N=64 Treatment

SYD985 in Patients With HER2-expressing Recurrent, Advanced or Metastatic Endometrial Carcinoma

Endometrial Cancer

Enrolled (actual)
64
Serious AEs
18.8%
Results posted
May 2024
Primary outcome: Primary: Objective Response Rate (ORR) — 20 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
SYD985 (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Byondis B.V.
Primary completion
Jan 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Objective Response Rate (ORR)
20
SECONDARY
Progression-Free Survival (PFS)
5.6
SECONDARY
Overall Survival (OS)
16.3
SECONDARY
Number of Participants With Treatment-Emergent Adverse Events (AEs)
51

Summary

The purpose of this study is to evaluate the safety and efficacy of SYD985 in recurrent, advanced or metastatic endometrial cancer.

Eligibility Criteria

Main Inclusion Criteria:

  • Females with histologically confirmed recurrent, advanced or metastatic endometrial carcinoma
  • Eligible patients should have progressed on or after first line platinum-based chemotherapy for advanced/metastatic endometrial cancer. Patients who have had two or more lines of chemotherapy for advanced/metastatic disease are not eligible, taking into account the following:
  • Patients may have received up to one additional line of chemotherapy if given in the neoadjuvant or adjuvant setting. If such treatment was completed less than 6 months prior to the current tumor recurrence or progression it is to be considered first-line treatment;
  • No more than one line of non-cytotoxic systemic cancer therapy (such as immunotherapy, trastuzumab or protein kinase inhibitors) is allowed.
  • HER2 tumor expression defined as a 1+, 2+ or 3+ score on IHC or positive by ISH
  • At least one measurable cancer lesion as defined by the Response Evaluation Criteria for Solid Tumours (RECIST version 1.1);
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2;

Exclusion Criteria

  • Current or previous use of a prohibited medication as listed in the protocol;
  • History of infusion-related reactions and/or hypersensitivity to trastuzumab;
  • History of keratitis;
  • Severe, uncontrolled systemic disease at screening;
  • Left Ventricular Ejection Fraction (LVEF) < 50%, or a history of clinically significant decrease in LVEF during previous treatment with trastuzumab;
  • History of clinically significant cardiovascular disease;
  • Symptomatic brain metastases, brain metastases requiring steroids to manage symptoms, or treatment for brain metastases within 8 weeks prior to randomization;
  • History or presence of idiopathic pulmonary fibrosis, organizing pneumonia (e.g. bronchiolitis obliterans), drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04205630). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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