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

Primary Purpose

Endometrial Cancer

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
SYD985
Sponsored by
Byondis B.V.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

  • Smilow Cancer Hospital (Yale)
  • Seoul National University Bundang Hospital
  • Seoul National University Hospital
  • Severance Hospital, Yonsei University Health System
  • Samsung Medical Center
  • The Catholic University of Korea, Seoul St. Mary's Hospital
  • MedTrials
  • St. John of Dukla Oncology Center of Lublin Land
  • Arkhangelsk Clinical Oncology Center
  • Chelyabinsk Regional Clinical Oncology and Nuclear Medicine Center
  • Regional Oncology Center
  • Clinical Oncology Center
  • Orenburg Regional Clinical Oncology Center
  • Private Medical Institution "EVROMEDSERVIS"
  • Oncology Center #2
  • Oncology Center of Moskovskiy District
  • AV Medical Group
  • Tambov Regional Oncological Clinical Center
  • Republican Clinical Oncology Center
  • Volgograd Regional Clinical Oncology Center
  • National Cancer Research Center
  • Clinical Center Nis, Clinic of Oncology
  • Oncology Institute of Vojvodina (IOV), Clinic of Surgical Oncology, Department of Gynecology
  • National University Hospital, Department of Hematology-Oncology
  • National Cancer Centre Singapore
  • Cherkasy Regional Oncology Dispensary of Cherkasy Oblast Council
  • Chernivtsi Regional Clinical Oncology Center
  • "City Clinical Hospital #4" under Dnipro City Council
  • Prykarpattia Clinical Oncology Center
  • State Institution: S.P. Hryhoriev Institute of Medical Radiology under the Ukrainian Academy of Medical Sciences
  • Communal Non-profit enterprise "Regional Center of Oncology"
  • Medical Center "Verum"
  • Odesa Regional Clinical Hospital
  • Public Non-Profit Enterprise Ternopil Regional Clinical Oncology Center
  • Podilla Regional Oncology Center
  • Medical Center ONCOLIFE LLC

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SYD985

Arm Description

SYD985, Intravenous, every 3 weeks (Q3W)

Outcomes

Primary Outcome Measures

Objective Response Rate (ORR)
Objective response rate is defined as the proportion of patients with an assessed best overall response of complete response or partial response according to Response Evaluation Criteria In Solid Tumors (RECIST) v1.1.

Secondary Outcome Measures

Progression-Free Survival (PFS)
Progression-free survival is defined as the time from the date of randomization to the date of first documented disease progression by investigator assessment according to RECIST v1.1 or death due to any cause, whichever occurred earlier.
Overall Survival (OS)
Overall survival is defined as the time from date of randomization to death due to any cause.
Incidence of Treatment-Emergent Adverse Events (AEs)
AEs will be graded by the investigator as assessed by CTCAE v5.0

Full Information

First Posted
December 12, 2019
Last Updated
May 15, 2023
Sponsor
Byondis B.V.
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1. Study Identification

Unique Protocol Identification Number
NCT04205630
Brief Title
SYD985 in Patients With HER2-expressing Recurrent, Advanced or Metastatic Endometrial Carcinoma
Official Title
A Single-arm Phase II Trial to Evaluate the Safety and Efficacy of the Antibody-Drug Conjugate (ADC) SYD985 in Patients With Human Epidermal Growth Factor Receptor 2 (HER2)-Expressing Endometrial Carcinoma Who Previously Progressed on or After First Line Platinum-based Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
May 28, 2020 (Actual)
Primary Completion Date
January 26, 2023 (Actual)
Study Completion Date
April 25, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Byondis B.V.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and efficacy of SYD985 in recurrent, advanced or metastatic endometrial cancer.
Detailed Description
This is an open-label, single-arm study in patients with HER2-expressing recurrent, advanced or metastatic endometrial carcinoma. HER2-expression is defined as a 1+, 2+ or 3+ score on immunohistochemistry (IHC) or positive by in situ hybridization (ISH). Eligible patients for this study should have progressed on or after first line platinum-based chemotherapy. Patients who have had two or more lines of chemotherapy for advanced/metastatic disease are not eligible. Eligible patients will receive SYD985 until disease progression or unacceptable toxicity. Patients who have stopped study treatment for other reasons than disease progression will continue their tumor evaluations in an observation period until disease progression or start of a new anticancer therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SYD985
Arm Type
Experimental
Arm Description
SYD985, Intravenous, every 3 weeks (Q3W)
Intervention Type
Drug
Intervention Name(s)
SYD985
Other Intervention Name(s)
Trastuzumab vc-seco-DUBA, (vic-)trastuzumab duocarmazine
Intervention Description
SYD985 powder for concentrate for solution for infusion
Primary Outcome Measure Information:
Title
Objective Response Rate (ORR)
Description
Objective response rate is defined as the proportion of patients with an assessed best overall response of complete response or partial response according to Response Evaluation Criteria In Solid Tumors (RECIST) v1.1.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Progression-Free Survival (PFS)
Description
Progression-free survival is defined as the time from the date of randomization to the date of first documented disease progression by investigator assessment according to RECIST v1.1 or death due to any cause, whichever occurred earlier.
Time Frame
2 years
Title
Overall Survival (OS)
Description
Overall survival is defined as the time from date of randomization to death due to any cause.
Time Frame
2-year overall survival
Title
Incidence of Treatment-Emergent Adverse Events (AEs)
Description
AEs will be graded by the investigator as assessed by CTCAE v5.0
Time Frame
2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norbert Koper
Organizational Affiliation
Byondis B.V., The Netherlands
Official's Role
Study Director
Facility Information:
Facility Name
Smilow Cancer Hospital (Yale)
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520-8063
Country
United States
Facility Name
Seoul National University Bundang Hospital
City
Seongnam-si
ZIP/Postal Code
13605
Country
Korea, Republic of
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
3080
Country
Korea, Republic of
Facility Name
Severance Hospital, Yonsei University Health System
City
Seoul
ZIP/Postal Code
3722
Country
Korea, Republic of
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
6351
Country
Korea, Republic of
Facility Name
The Catholic University of Korea, Seoul St. Mary's Hospital
City
Seoul
ZIP/Postal Code
6591
Country
Korea, Republic of
Facility Name
MedTrials
City
Kraków
ZIP/Postal Code
30-820
Country
Poland
Facility Name
St. John of Dukla Oncology Center of Lublin Land
City
Lublin
ZIP/Postal Code
20-090
Country
Poland
Facility Name
Arkhangelsk Clinical Oncology Center
City
Arkhangelsk
ZIP/Postal Code
163045
Country
Russian Federation
Facility Name
Chelyabinsk Regional Clinical Oncology and Nuclear Medicine Center
City
Chelyabinsk
ZIP/Postal Code
454087
Country
Russian Federation
Facility Name
Regional Oncology Center
City
Irkutsk
ZIP/Postal Code
664035
Country
Russian Federation
Facility Name
Clinical Oncology Center
City
Omsk
ZIP/Postal Code
644013
Country
Russian Federation
Facility Name
Orenburg Regional Clinical Oncology Center
City
Orenburg
ZIP/Postal Code
460021
Country
Russian Federation
Facility Name
Private Medical Institution "EVROMEDSERVIS"
City
Saint Petersburg
ZIP/Postal Code
196603
Country
Russian Federation
Facility Name
Oncology Center #2
City
Sochi
ZIP/Postal Code
354057
Country
Russian Federation
Facility Name
Oncology Center of Moskovskiy District
City
St. Petersburg
ZIP/Postal Code
196247
Country
Russian Federation
Facility Name
AV Medical Group
City
St. Petersburg
ZIP/Postal Code
197082
Country
Russian Federation
Facility Name
Tambov Regional Oncological Clinical Center
City
Tambov
ZIP/Postal Code
392013
Country
Russian Federation
Facility Name
Republican Clinical Oncology Center
City
Ufa
ZIP/Postal Code
450054
Country
Russian Federation
Facility Name
Volgograd Regional Clinical Oncology Center
City
Volgograd
ZIP/Postal Code
400138
Country
Russian Federation
Facility Name
National Cancer Research Center
City
Belgrade
ZIP/Postal Code
11000
Country
Serbia
Facility Name
Clinical Center Nis, Clinic of Oncology
City
Nis
ZIP/Postal Code
18000
Country
Serbia
Facility Name
Oncology Institute of Vojvodina (IOV), Clinic of Surgical Oncology, Department of Gynecology
City
Sremska Kamenica
ZIP/Postal Code
21204
Country
Serbia
Facility Name
National University Hospital, Department of Hematology-Oncology
City
Singapore
ZIP/Postal Code
119074
Country
Singapore
Facility Name
National Cancer Centre Singapore
City
Singapore
ZIP/Postal Code
169610
Country
Singapore
Facility Name
Cherkasy Regional Oncology Dispensary of Cherkasy Oblast Council
City
Cherkasy
ZIP/Postal Code
18099
Country
Ukraine
Facility Name
Chernivtsi Regional Clinical Oncology Center
City
Chernivtsi
ZIP/Postal Code
58013
Country
Ukraine
Facility Name
"City Clinical Hospital #4" under Dnipro City Council
City
Dnipro
ZIP/Postal Code
49102
Country
Ukraine
Facility Name
Prykarpattia Clinical Oncology Center
City
Ivano-Frankivsk
ZIP/Postal Code
76018
Country
Ukraine
Facility Name
State Institution: S.P. Hryhoriev Institute of Medical Radiology under the Ukrainian Academy of Medical Sciences
City
Kharkiv
ZIP/Postal Code
61024
Country
Ukraine
Facility Name
Communal Non-profit enterprise "Regional Center of Oncology"
City
Kharkiv
ZIP/Postal Code
61070
Country
Ukraine
Facility Name
Medical Center "Verum"
City
Kyiv
ZIP/Postal Code
3039
Country
Ukraine
Facility Name
Odesa Regional Clinical Hospital
City
Odesa
ZIP/Postal Code
65025
Country
Ukraine
Facility Name
Public Non-Profit Enterprise Ternopil Regional Clinical Oncology Center
City
Ternopil
ZIP/Postal Code
46023
Country
Ukraine
Facility Name
Podilla Regional Oncology Center
City
Vinnytsia
ZIP/Postal Code
21029
Country
Ukraine
Facility Name
Medical Center ONCOLIFE LLC
City
Zaporizhzhia
ZIP/Postal Code
69059
Country
Ukraine

12. IPD Sharing Statement

Plan to Share IPD
No

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

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