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A Study of Raludotatug Deruxtecan (R-DXd) With or Without Bevacizumab as Maintenance Therapy in Second-Line Platinum-Sensitive Recurrent Ovarian Cancer (REJOICE-Ovarian03)

31 augusti 2026 uppdaterad av: Daiichi Sankyo

A Phase 3, Multicenter, Randomized, Open-Label Trial of Raludotatug Deruxtecan With or Without Bevacizumab as Maintenance Therapy Versus Standard of Care in Participants With First Recurrence Platinum-Sensitive, High-Grade Serous or Endometrioid Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancer (REJOICE-Ovarian03)

The primary purpose of the study is to evaluate the efficacy of R-DXd with or without bevacizumab as maintenance therapy compared with standard of care (SOC) in participants with platinum-sensitive ovarian cancer (PSOC) as measured by progression-free survival (PFS) as assessed by Blinded Independent Central Review (BICR).

Studieöversikt

Studietyp

Interventionell

Inskrivning (Beräknad)

600

Fas

  • Fas 3

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria

  1. Adult participants with assigned female sex at birth.
  2. Participants with histologically or cytologically documented high-grade (Grade 3) serous or endometrioid epithelial ovarian cancer (OVC), primary peritoneal cancer, or fallopian tube cancer.
  3. Has an homologous recombinant deficiency (HRD) or breast cancer gene (BRCA) test result using a validated or approved test as per applicable regulations available.
  4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
  5. Required baseline local laboratory data (within 7 days prior to randomization) as specified in the protocol.
  6. A woman of childbearing potential (WOCBP), as specified in the protocol, is eligible to participate if the protocol-specified conditions are met.
  7. Must have received 2 prior lines of platinum-based therapy:

    • For the first-line (1L) platinum-based chemotherapy (penultimate, platinum-based course prior to enrollment on the trial), must have platinum-sensitive disease after this treatment, defined as documented radiologic disease progression assessed by the investigator (evident measurable or non-measurable disease according to RECIST v1.1) >6 months following the last dose of the platinum administered.
    • For the second (last) platinum-based chemotherapy course prior to enrollment on the trial, must have received a platinum-containing regimen for a minimum of 4 cycles and a maximum of 8 cycles.
  8. Must have achieved evidence of non-progressive radiological disease based on investigator-assessed RECIST 1.1 and CA-125 at the end of induction treatment with platinum-based doublet chemotherapy (no evidence of disease [NED], complete response [CR], partial response [PR] or stable disease [SD] for participants with measurable disease at baseline; or NED, CR, or non-CR/non-progressive disease [PD] for participants with non-measurable disease based on RECIST v1.1).
  9. According to investigator assessment, polymerase inhibitor (PARPi) as 2L maintenance treatment is not the preferred option for the participant.
  10. Must be randomized between 4 and 9 weeks after completion of their final dose of the platinum-containing regimen.
  11. Is willing and able to comply with scheduled visits, drug administration plan, laboratory tests, other trial procedures, and trial restrictions.

Exclusion Criteria:

  1. Non-serous or non-endometrioid high-grade epithelial histology, or non-epithelial tumor origin of the ovary, the fallopian tube or the peritoneum (i.e., germ cell tumors) or low-grade/borderline OVC.
  2. Inadequate washout period before randomization, defined as follows:

    • Major surgery less than (<)28 days.
    • Radiation therapy less than equal to (≤)28 days (if palliative stereotactic radiation therapy without abdominal radiation, ≤14 days).
    • Systemic anticancer therapy (including but not limited to antibody-drug therapy, retinoid therapy, and hormonal therapy) <28 days or 5 half-lives, whichever is shorter, before starting trial intervention or current participation in other therapeutic investigational procedures.
    • Chloroquine/hydroxychloroquine ≤14 days.
    • Exposure to another investigational trial intervention within 28 days prior to start of trial intervention or current participation in other therapeutic investigational procedures.
  3. Clinically active brain metastases, spinal cord compression, or leptomeningeal carcinomatosis, defined as untreated or symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms. Participants with untreated and asymptomatic brain metastases or participants with previously treated brain metastases who are no longer symptomatic and who require no treatment with steroids may be included in the trial if they have recovered from the acute toxic effect of radiotherapy, at the investigator's discretion. A minimum of 2 weeks must have elapsed between the end of radiotherapy and trial intervention and there should be no evidence of progression or need for steroids treatment or anticonvulsants for at least 2 weeks prior to randomization.
  4. Any of the following within the past 6 months prior to randomization: cerebrovascular accident, transient ischemic attack, other arterial thromboembolic event (e.g., intestinal ischemia).
  5. Uncontrolled or significant cardiovascular disease:

    • QTcF interval >470 milliseconds (ms).
    • Diagnosed or suspected long QT syndrome.
    • History of clinically relevant ventricular arrhythmias, such as ventricular tachycardia, ventricular fibrillation, or Torsade de Pointes.
    • Participant has clinically relevant bradycardia of less than 50 beats per minute (bpm), unless the participant has a pacemaker.
    • History of second- or third-degree heart block. Candidates with a history of heart block may be eligible if they currently have pacemakers and have no history of fainting or clinically relevant arrhythmia with pacemakers.
    • Myocardial infarction within 6 months prior to screening.
    • Uncontrolled angina pectoris within 6 months prior to screening.
    • New York Heart Association (NYHA) Class 3 or 4 congestive heart failure (CHF).
    • Left ventricular ejection fraction <50% or institutional lower limit of normal as measured by echocardiography or multigated acquisition scan (MUGA) scan.
    • Coronary/peripheral artery bypass graft within 6 months prior to screening.
    • Prior history of hypertensive crisis (common terminology criteria for adverse events [CTCAE] Grade 4) or hypertensive encephalopathy or uncontrolled hypertension CTCAE Grade greater than equal to (≥)3 hypertension as per National Cancer Institute (NCI) CTCAE version 6.0.
    • Complete left or right bundle branch block.
  6. Has any history of interstitial lung disease (ILD)/pneumonitis irrespective of steroid use, or current ILD, or suspected ILD, or ILD that cannot be ruled out by imaging at screening. Participants may be eligible if they had history of radiation pneumonitis that did not require steroids. Examples of suspected ILD/pneumonitis by imaging include the presence of lung parenchymal fibrosis, such as combined pulmonary fibrosis and emphysema (CPFE), and any radiographic features consistent with ILA, including but not limited to extensive ground glass opacities, reticular opacities, traction bronchiectasis, and honeycombing.
  7. Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder (i.e., pulmonary emboli within 3 months of the trial enrollment, severe asthma, severe COPD, restrictive lung disease, pleural effusion, etc.) and any autoimmune, connective tissue, or inflammatory disorders with potential pulmonary involvement (e.g., rheumatoid arthritis, Sjogren's syndrome, sarcoidosis, etc.), or prior pneumonectomy.
  8. Chronic steroid treatment (>10 mg/day prednisone [or equivalent] per day), with the exception of the following:

    • Inhaled steroids for asthma or chronic obstructive pulmonary disease (COPD).
    • Mineralocorticoids (e.g., fludrocortisone) for participants with orthostatic hypotension.
    • Topical steroids for mild skin conditions.
    • Low-dose supplemental corticosteroids for adrenocortical insufficiency.
    • Premedication for treatment groups and/or premedication in case of any hypersensitivity.
    • Intra-articular steroid injections.
  9. History of malignancy other than epithelial OVC, primary peritoneal cancer, or fallopian tube cancer within 3 years prior to randomization, with the exception of those with a negligible risk of metastasis or death (e.g., 5-year OS rate >90%) and treated with expected curative outcome (such as adequately treated carcinoma in situ of the cervix, nonmelanoma skin carcinoma, ductal carcinoma in situ, or Stage 1 uterine cancer).
  10. Unresolved toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet resolved to NCI CTCAE version 6.0, Grade ≤1 or baseline.
  11. Has current, clinically relevant bowel obstruction (including subocclusive disease) including obstruction related to underlying epithelial OVC, abdominal fistula or gastrointestinal perforation, intra-abdominal abscess.
  12. History of severe hypersensitivity (≥ Grade 3) or any known contraindication to R-DXd or any excipients in R-DXd.
  13. Has active or uncontrolled Human Immunodeficiency Virus (HIV) infection.
  14. Has any evidence of severe or uncontrolled systemic diseases (including active bleeding diatheses or active infection, substance abuse) or other factors that, in the investigator's opinion, makes it undesirable for the participant to participate in the trial or which would jeopardize compliance with the protocol. Screening for chronic conditions is not required;
  15. Has active or uncontrolled HBV infection. Hepatitis B screening testing is required.
  16. Has active or uncontrolled hepatitis C virus (HCV) infection. Hepatitis C screening testing is required.
  17. Female who is pregnant or breastfeeding or intends to become pregnant during the trial.
  18. Psychological, social, familial, or geographical factors that would prevent regular follow-up (FU).
  19. Has a history of receiving live-attenuated vaccine (messenger ribonucleic acid [mRNA] and replication-deficient adenoviral vaccines are not considered attenuated live vaccines) within 30 days prior to the first exposure to trial intervention.
  20. Participants are ineligible if they have a history of any contraindication included in the approved local label for the control group treatment.

    Additional Exclusion Criteria for Bevacizumab Participants:

  21. Has a history of arterial thromboembolic events, hemorrhage, hemoptysis, active gastrointestinal bleeding that occurred within 6 months before randomization.
  22. Participants with history of serious, non-healing wound, active ulcer or untreated bone fracture.
  23. History of vascular endothelial growth factor (VEGF) therapy related abdominal fistula or gastrointestinal perforation.
  24. Participants who discontinued bevacizumab during the second (last) platinum-based chemotherapy due to any AE related to bevacizumab are not eligible to receive bevacizumab.
  25. Severe hypersensitivity (≥Grade 3) to bevacizumab and/or any of its excipients. Participants with known sensitivity to Chinese Hamster Ovary cell products or other recombinant human or humanized antibodies are prohibited from receiving bevacizumab during the trial.
  26. Participants who have had a major surgical procedure, open biopsy, dental extractions or other dental surgery/procedure that results in an open wound, or significant traumatic injury (e.g., long-bone fracture requiring surgery) as per investigator judgment within 28 days prior to the first date of treatment on this trial, or anticipation of need for major surgical procedure during the course of the trial; participants with placement of vascular access device or core biopsy within 7 days prior to the first date of treatment in the trial.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Arm 1: R-DXd Alone or R-DXd Combined with Bevacizumab
Participants will be randomized to receive either R-DXd, intravenously (IV), every 3 weeks (Q3W) alone, or R-DXd IV along with bevacizumab 15mg/kg, IV, Q3W, on Day 1 of each 21-day cycle, until radiological disease progression according to RECIST v1.1 as assessed by BICR, unacceptable toxicity or other protocol-specified discontinuation criteria are met.
R-DXd will be administered as an intravenous (IV) infusion.
Andra namn:
  • DS-6000a
Bevacizumab will be administered as an IV infusion.
Andra namn:
  • MVASI
  • AVASTIN®
Aktiv komparator: Arm 2: Bevacizumab Alone or Observation
Participants will be randomized to receive either bevacizumab 15 mg/kg, IV, Q3W, or Investigator's choice of observation until radiological disease progression as assessed by BICR or unacceptable toxicity or until other protocol-specified discontinuation criteria are met.
Bevacizumab will be administered as an IV infusion.
Andra namn:
  • MVASI
  • AVASTIN®

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Progression Free Survival (PFS) as Assessed by Blinded Independent Central Review (BICR) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1)
Tidsram: Up to approximately 6 years
PFS is defined as the time (month) from the date of randomization to the earlier date of the first objective documentation of radiographic disease progression as assessed by BICR per RECIST v1.1 or death due to any cause.
Up to approximately 6 years

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Overall Survival (OS)
Tidsram: Up to approximately 6 years
OS is defined as the time (month) from the date of randomization to the date of death due to any cause.
Up to approximately 6 years
PFS as Assessed by Investigator per RECIST v1.1
Tidsram: Up to approximately 6 years
PFS is defined as the time (month) from the date of randomization to the earlier date of the first objective documentation of radiological disease progression as assessed by the investigator per RECIST v1.1 or death due to any cause.
Up to approximately 6 years
Progression Free Survival 2 (PFS2)
Tidsram: Up to approximately 6 years
PFS2 is defined as the time (in months) from the date of randomization to the earlier date of the second disease progression, or death due to any cause.
Up to approximately 6 years
Number of Participants With at Least One Treatment-emergent Adverse Event (TEAE)
Tidsram: Up to approximately 6 years
TEAEs are defined as those adverse events (AEs) with a start or worsening date during the on-treatment period (from the first dose date to 70 days after the last dose date of study treatment).
Up to approximately 6 years
Plasma Concentrations of R-DXd (Conjugated Antibody)
Tidsram: Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Plasma Concentrations of Total Anti-Cadherin-6 (CDH6) Antibody
Tidsram: Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Plasma Concentrations of DXd Payload
Tidsram: Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Percentage of Participants Having Treatment-Emergent Antidrug Antibody (ADA)
Tidsram: Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
Pre-dose and post-dose at multiple timepoints during each cycle, up to approximately 6 years (Cycle length=21 days)
CDH6 Protein Expression in Tumor Tissue as Determined by Immunochemistry Assay (Immunohistochemistry [IHC]) and Correlation with PFS and OS
Tidsram: Up to approximately 6 years
Up to approximately 6 years
Change From Baseline in Global Health Status/Quality of Life (QoL) Assessed by European Organisation for Research and Treatment of Cancer Core Quality of Life Questionnaire Version 3.0 (EORTC QLQ-C30 v3.0)
Tidsram: Baseline up to approximately 6 years
The EORTC QLQ-C30 assesses 5 functional scales, 3 symptom scales, a global health/QoL scale, and 6 single items. Change in QOLwill be assessed using 2 global health/QoL items scored on a 7-point scale ranging from 1 ("very poor") to 7 ("excellent"). Scores are linearly transformed on a scale 0 to 100. A high scale score represents a better QoL.
Baseline up to approximately 6 years
Change From Baseline in Functional Sub-scales Scores Assessed by EORTC QLQ-C30 v3.0
Tidsram: Baseline up to approximately 6 years
The EORTC QLQ-C30 assesses 5 functional scales, 3 symptom scales, a global health/QoL scale, and 6 single items. The functional items are scored on a 4-point scale ranging from 1 ("not at all") to 4 ("very much"). Scores are linearly transformed on a scale 0 to 100. A high scale score represents a better functioning.
Baseline up to approximately 6 years
Change From Baseline in Symptom Sub-scales Score Assessed by EORTC QLQ-C30 v3.0
Tidsram: Baseline up to approximately 6 years
The EORTC QLQ-C30 assesses 5 functional scales, 3 symptom scales, a global health/QoL scale, and 6 single items. The symptom items are scored on a 4-point scale ranging from 1 ("not at all") to 4 ("very much"). Scores are linearly transformed on a scale 0 to 100. A high scale score represents worst symptoms.
Baseline up to approximately 6 years
Time to Deterioration (TTD) in Global Health Scale/QoL, Functioning and Symptoms as Measured by EORTC QLQ-C30 v3.0
Tidsram: Up to approximately 6 years
The EORTC QLQ-C30 assesses 5 functional scales, 3 symptom scales, a global health/QoL scale, and 6 single items. The functional, symptom and single items are scored on a 4-point scale ranging from 1 ("not at all") to 4 ("very much"). The final 2 global health/QoL items are scored on a 7-point scale ranging from 1 ("very poor") to 7 ("excellent"). All of the scales and single-item measures scores are linearly transformed on a scale 0 to 100. A high scale score represents a higher response level and worst symptoms for the symptom scales.
Up to approximately 6 years
Change From Baseline in Abdominal/Gastrointestinal (GI) Symptoms Assessed by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Ovarian Cancer Module (EORTC QLQ-OV28)
Tidsram: Baseline up to approximately 6 years
The EORTC QLQ-OV28 consists of 28 items assessing abdominal/GI symptoms (6 items), peripheral neuropathy (2 items), other chemotherapy side effects (5 items), hormonal symptoms (2 items), body image (2 items), attitudes to disease/treatment (3 items), sexuality (4 items), indigestion/heartburn (1 item), hair loss (2 items), and change in taste (1 item). All scores range from 0 to 100, with a higher score indicating a worse outcome, except for the sexuality domain, where this is reversed.
Baseline up to approximately 6 years
Change From Baseline in Attitude to Disease/Treatment Assessed by EORTC QLQ-OV28
Tidsram: Baseline up to approximately 6 years
The EORTC QLQ-OV28 consists of 28 items assessing abdominal/GI symptoms (6 items), peripheral neuropathy (2 items), other chemotherapy side effects (5 items), hormonal symptoms (2 items), body image (2 items), attitudes to disease/treatment (3 items), sexuality (4 items), indigestion/heartburn (1 item), hair loss (2 items), and change in taste (1 item). All scores range from 0 to 100, with a higher score indicating a worse outcome, except for the sexuality domain, where this is reversed.
Baseline up to approximately 6 years
TTD in Abdominal/GI Symptoms and Attitude to Disease/Treatment as Measured by EORTC QLQ-OV28
Tidsram: Up to approximately 6 years
The EORTC QLQ-OV28 consists of 28 items assessing abdominal/GI symptoms (6 items), peripheral neuropathy (2 items), other chemotherapy side effects (5 items), hormonal symptoms (2 items), body image (2 items), attitudes to disease/treatment (3 items), sexuality (4 items), indigestion/heartburn (1 item), hair loss (2 items), and change in taste (1 item). All scores range from 0 to 100, with a higher score indicating a worse outcome, except for the sexuality domain, where this is reversed.
Up to approximately 6 years

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Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 oktober 2026

Primärt slutförande (Beräknad)

1 juli 2029

Avslutad studie (Beräknad)

1 december 2033

Studieregistreringsdatum

Först inskickad

3 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

24 augusti 2026

Första postat (Faktisk)

28 augusti 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

1 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

31 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

JA

IPD-planbeskrivning

De-identified individual participant data (IPD) on completed studies and applicable supporting clinical trial documents may be available upon request at https://vivli.org/. In cases where clinical trial data and supporting documents are provided pursuant to our company policies and procedures, Daiichi Sankyo will continue to protect the privacy of our clinical trial participants. Details on data sharing criteria and the procedure for requesting access can be found at this web address: https://vivli.org/ourmember/daiichi-sankyo/

Tidsram för IPD-delning

Completed studies that have reached a global end or completion with all data set collected and analyzed, and for which the medicine and indication have received European Union (EU) and United States (US), and/or Japan (JP) marketing approval on or after 01 January 2014 or by the US or EU or JP Health Authorities when regulatory submissions in all regions are not planned and after the primary study results have been accepted for publication.

Kriterier för IPD Sharing Access

Formal request from qualified scientific and medical researchers on IPD and clinical study documents on completed clinical trials supporting products submitted and licensed in the United States, the European Union and/or Japan from 01 January 2014 and beyond for the purpose of conducting legitimate research. This must be consistent with the principle of safeguarding study participants' privacy and consistent with provision of informed consent.

IPD-delning som stöder informationstyp

  • STUDY_PROTOCOL
  • SAV
  • ICF

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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