Phase 2
N=64
SYD985 in Patients With HER2-expressing Recurrent, Advanced or Metastatic Endometrial Carcinoma
Endometrial Cancer
Bottom Line
View on ClinicalTrials.gov: NCT04205630 ↗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
| Outcome | Result | p-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.
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.