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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 agosto 2026 aggiornato da: 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).

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

600

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Altri nomi:
  • DS-6000a
Bevacizumab will be administered as an IV infusion.
Altri nomi:
  • MVASI
  • AVASTIN®
Comparatore attivo: 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.
Altri nomi:
  • MVASI
  • AVASTIN®

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
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)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall Survival (OS)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 ottobre 2026

Completamento primario (Stimato)

1 luglio 2029

Completamento dello studio (Stimato)

1 dicembre 2033

Date di iscrizione allo studio

Primo inviato

3 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

24 agosto 2026

Primo Inserito (Effettivo)

28 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

1 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

31 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

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/

Periodo di condivisione IPD

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.

Criteri di accesso alla condivisione IPD

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.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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