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Phase 2 Completed N=64 Treatment

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

Source: ClinicalTrials.gov NCT04205630 ↗
Enrolled (actual)
64
Serious AEs
18.8%
Results posted
May 2024
Primary outcomePrimary: Objective Response Rate (ORR) — 20 Participants

Summary

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

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

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. Informational only — not medical advice.

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