このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Safety and Efficacy of Ubamatamab With First-line Chemotherapy in Ovarian Cancer (RegeNovar)

2026年7月9日 更新者:ARCAGY/ GINECO GROUP

A Phase I/II Study of Ubamatamab Plus Carboplatin, Paclitaxel, and Bevacizumab as Salvage Therapy in Ovarian Cancer With Poor Response to First-Line Chemotherapy

The purpose of this clinical trial is to assess the safety and efficacy of ubamatamab in combination with first-line chemotherapy in patients with ovarian cancer. The main questions it aims to answer are:

  • What is the safety profile of ubamatamab when administered with carboplatin-paclitaxel ± bevacizumab?
  • What is the objective response rate after three cycles of ubamatamab in combination with carboplatin-paclitaxel ± bevacizumab?

Participants will:

  • Receive three cycles of ubamatamab in combination with carboplatin-paclitaxel ± bevacizumab, followed by maintenance therapy with ubamatamab ± bevacizumab for up to 15 months, depending on HRD status and disease response after the initial treatment cycles.
  • Attend regular clinic visits throughout the treatment period for checkups and tests

調査の概要

状態

まだ募集していません

条件

研究の種類

介入

入学 (推定)

43

段階

  • フェーズ2
  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Bordeaux、フランス、33076
        • Institut Bergonie
        • 主任研究者:
          • Coriolan Lebreton
      • Caen、フランス、14076
        • Centre François Baclesse
        • 主任研究者:
          • Coraline DUBOT POITELON
      • Dijon、フランス、21079
        • Centre Georges François Leclerc
        • 主任研究者:
          • Leïla BENGRINE LEFEVRE
      • Lyon、フランス、69373
        • Centre Léon Bérard
        • 主任研究者:
          • Brunhilde HANVIC
      • Marseille、フランス、13273
        • Institut Paoli Calmettes
        • 主任研究者:
          • Renaud SABATIER
      • Montpellier、フランス、34298
        • ICM Val d'Aurelle
        • 主任研究者:
          • Stanislas QUESADA
      • Pierre-Bénite、フランス、69495
        • HCL - Centre Hospitalier Lyon Sud
        • 主任研究者:
          • BENOIT YOU
      • Rennes、フランス、35042
        • Centre Eugene Marquis
        • 主任研究者:
          • Thibault DE LA MOTTE ROUGE
      • Saint-Herblain、フランス、44805
        • ICO - Centre René Gauducheau
        • 主任研究者:
          • Jean-Sébastien Frenel
      • Strasbourg、フランス、67098
        • Hôpital de Hautepierre
        • 主任研究者:
          • Laurianne EBERST
      • Villejuif、フランス、94805
        • Gustave Roussy
        • 主任研究者:
          • Alexandra LEARY

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Histologically confirmed high-grade epithelial (serous, endometrioid, or carcinosarcoma with a ≥30% epithelial tumor component) ovarian, primary peritoneal, or fallopian-tube carcinoma
  2. Adult patient aged ≥ 18 years old
  3. Advanced stage III or IV
  4. Treated with 3 or 4 standard neo-adjuvant cycles of carboplatin-paclitaxel regimen, in first line, given every 3 weeks, and characterized by 2 unfavorable features (both are required):

    • A poorly chemosensitive disease defined by an unfavorable standardized KELIM score < 1.0 calculated on CA-125 KELIM™ calculator for patients treated with neo-adjuvant chemotherapy
    • A disease considered not amenable to complete interval cytoreductive surgery with no post-operative macroscopic residual lesion (either because the interval cytoreductive surgery attempt was incomplete CC2-CC3, or because the surgeon considers a complete interval cytoreductive surgery is not achievable based on imaging and/or laparoscopic explorations)
  5. Disease measurable and assessable by imaging based on RECIST 1.1 criteria (thorax-abdomen-pelvis CT-scanner; FDG-PET-CT-scanner; and/or MRI)
  6. Availability of a tumor tissue for translational research (archival tissue, or alternatively from fresh biopsy, and/or surgery)
  7. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  8. BRCA and HRD status known, or planned during the trial (before maintenance treatment)
  9. Adequate bone marrow function

    • Red blood cells: baseline Hemoglobin ≥8 g/dL (without red blood cell transfusion within 3 weeks before the blood work)
    • White blood cells: Absolute neutrophil count (ANC) ≥1500 cells/mm3
    • Platelets: Platelet count ≥100,000/mm3
  10. Adequate renal and liver functions

    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × upper limit of normal (ULN), or ≤5 × ULN in context of liver metastases
    • Total bilirubin ≤1.5 × ULN (patients with Gilbert's are eligible if total bilirubin ≤3 × ULN)
    • Albumin ≥3 g/dL
    • Creatinine clearance ≥40 mL/min/1.73 m2 (measured or estimated, ideally with CKD-EPI formula on https://www.kidney.org/professionals/kdoqi/gfr_calculator )
  11. Adequate heart function: LVEF ≥ 50%, measured by echocardiogram, and troponin levels above the upper limit of normal (ULN). The case of troponin level comprised between 1.0 and 2 ULN, inclusion may be discussed after cardiological assessment.
  12. Life expectancy of at least 3 months
  13. Patients who gave their written informed consent to participate to the study
  14. Patients affiliated to a social insurance regime
  15. Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow-up.

Non-inclusion Criteria:

  1. Low-grade endometrioid, clear cell, mucinous, or sarcomatous histology, or mixed tumors containing any of these histologies, or low-grade or borderline ovarian tumor.
  2. Patients with primary platinum-refractory disease, defined as disease that has radiologically progressed during the neo-adjuvant chemotherapy
  3. Contraindication to ubamatamab
  4. Contraindication to carboplatin, paclitaxel or bevacizumab
  5. Previous treatment with bevacizumab during initial standard neo-adjuvant chemotherapy
  6. Prior treatment with anti-PD-1 therapies or T-cell therapies, or any other experimental anti-cancer systemic therapy
  7. Patients with second primary cancer, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumors curatively treated with no evidence of disease for ≥ 2 years.
  8. All trial participants with brain metastases, except those meeting the following criteria (all criteria are required):

    1. Brain metastases that have been treated locally, and are clinically asymptomatic for at least 4 weeks prior to enrolment,
    2. No ongoing neurological symptoms that are related to the brain localization of the disease (sequelae that are a consequence of the treatment of the brain metastases are acceptable).
    3. Trial participants with brain metastases must be either off steroids except a stable or decreasing dose of <10mg daily prednisone (or equivalent).
  9. Encephalitis, meningitis, or uncontrolled seizures in the year prior to informed consent
  10. Patients receiving any systemic chemotherapy, radiotherapy (except for symptomatic/palliative reasons), within 3 weeks before the first dose of ubamatamab. The patient can receive a stable dose of bisphosphonates for bone metastases, before and during the study if these were started at least 4 weeks prior to treatment with study drug.
  11. Persistent toxicities (≥CTCAE grade 3), caused by previous cancer therapy
  12. Treatment with other investigational agents.
  13. Bowel occlusive syndrome, inflammatory bowel disease, immune colitis, or other gastro-intestinal disorder that does not allow oral medication, such as malabsorption.
  14. Clinically significant (i.e., active) and severe cardiovascular disease according to investigator opinion such as myocardial infarction (< 6 months prior to enrollment); any history of myocarditis; significant arrhythmia including paroxysmal atrial fibrillation requiring intervention at any time or implantation of a pacemaker or defibrillator; signs or symptoms of active angina; arrhythmia or heart failure; LEVF < 50% with echocardiogram; QTc (Friedericia) interval >470 msec (in cases of asymptomatic prolonged QTc interval (>470 msec), the ECG can be repeated up to 2 times. If subsequent QTc interval is <470 msec, the patient may be enrolled but only after review and approval by a cardiologist); Evidence of Second-Degree AV block type II (Mobitz type II) or AV block type III (complete heart block); Baseline serum troponin above institutional upper limit of normal. In cases of minimally elevated troponin in absence of clinical symptoms, after clearance by a cardiologist, the patient may be enrolled.
  15. Untreated pulmonary embolism (PE) or deep vein thrombosis (DVT), not currently managed with anticoagulant therapy. Ongoing or recent (within 5 years) evidence of significant autoimmune disease that required treatment with systemic immunosuppressive treatments, which may suggest risk for immunological adverse events. The following are not exclusionary: vitiligo, childhood asthma that has resolved, hypothyroidism that required only hormone replacement, type 1 diabetes or psoriasis that does not require systemic treatment
  16. Uncontrolled infection with human immunodeficiency virus, hepatitis B or hepatitis C infection; or diagnosis of immunodeficiency or known latent tuberculosis infection.

    Participants will be tested for HCV and HBV at screening per Section 5.2

    • Patients with HIV who have controlled infection (undetectable viral load and CD4 count above 350 either spontaneously or on a stable antiviral regimen) are permitted.
    • Patients with hepatitis B surface antigen positive (HepBsAg+) who have controlled infection (serum hepatitis B virus DNA PCR that is below the limit of detection AND receiving antiviral therapy for hepatitis B) are permitted.
    • Participants with HBsAg negative but total HBV core antibody positive (HBc Ab+) are permitted with the following requirements: If serum HBV DNA PCR is above the limit of detection at screening, antiviral therapy for HBV must be initiated prior to study entry. If serum HBV DNA PCR is below the limit of detection periodic monitoring of HBsAg must be performed.
    • Patients who are Hepatitis C virus antibody positive (HCV Ab +) who have controlled infection (undetectable HCV RNA by PCR either spontaneously or in response to a successful prior course of anti-HCV therapy) are permitted.
  17. Other active infections requiring hospitalization or IV anti-infectives within 2 weeks before starting study treatment.
  18. Receipt of a live vaccine within 30 days of planned start of study medication.
  19. Pregnant or lactating patients or patients expecting to conceive children within the projected duration of the trial.
  20. Women of childbearing potential (WOCBP)* who are unwilling to practice highly effective contraception prior to the initial dose/start of the first treatment, during the study, and for at least 6 months after the last dose. Highly effective contraceptive measures include:

    1. stable use of combined (estrogen and progestogen containing) hormonal contraception (oral, intravaginal, transdermal) or progestogen-only hormonal contraception (oral, injectable, implantable) associated with inhibition of ovulation initiated 2 or more menstrual cycles prior to screening
    2. intrauterine device (IUD); intrauterine hormone-releasing system (IUS)
    3. bilateral tubal occlusion/ligation
    4. vasectomized partner (provided that the male vasectomized partner is the sole sexual partner of the study participant and that the vasectomized partner has obtained medical assessment of surgical success for the procedure) and/or e. sexual abstinence** *** * WOCBP are defined as women who are fertile following menarche until becoming postmenopausal, unless permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy.

    A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. A high follicle-stimulating hormone (FSH) level in the postmenopausal range may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient to determine the occurrence of a postmenopausal state. The above definitions are according to Clinical Trial Facilitation Group (CTFG) guidance.

    ** Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient.

    ***Periodic abstinence (calendar, symptothermal, post-ovulation methods), withdrawal (coitus interruptus), spermicides only, and lactational amenorrhea method (LAM) are not acceptable methods of contraception. Female condom and male condom should not be used together.

  21. Known psychiatric disorder that would interfere with trial compliance.
  22. Patient deprived of liberty, under guardianship, or under curatorship

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Carboplatin-paclitaxel-bevacizumab + ubamatamab

All participants will receive 3 cycles of the combination carboplatin-paclitaxel-bevacizumab + ubamatamab. After the 3 cycles, they will undergo surgery if it is feasible. Subsequently, they will receive maintenance treatment:

  • ubamatamab + bevacizumab: for participants with BRCA wild-type and HRD negative tumors and for participants with a disease characterized by a BRCA mutation, or HRD positive status, and experiencing stable disease during the chemotherapy
  • Olaparib + bevacizumab (standard of care): for participants with a disease characterized by a BRCA mutation, or HRD-positive status, and experiencing complete or partial response during the chemotherapy.
Dosage form: Solution for perfusion Dosage: 5 mg/mL; 50 mg/mL Frequency: administration every three weeks Treatment duration: 15 months
Carboplatin + Paclitaxel administered at each cycle of 21 days (in total 3 cycles).
Bevacizumab administered at each cycle of 21 days (3 cycles in total) then during maintenance therapy every 3 weeks.
Administered at each cycle during the 3 first cycles of the drug combination (chemotherapy + bevacizumab + ubamatamab).

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Safety run-in phase I : Safety and recommended dose for phase II trial during the Dose-limiting toxicities monitoring period
時間枠:Up to 4 weeks of treatment
Incidence of Treatment emergent adverse events according to NCI CTCAE version 6.0 (Safety and Tolerability)
Up to 4 weeks of treatment
Safety run-in phase I : Safety and recommended dose for phase II trial during the Dose-limiting toxicities monitoring period
時間枠:Up to 4 weeks of treatment
Dose-limiting toxicities (DLT) occurring during the DLT period (Safety and Tolerability)
Up to 4 weeks of treatment
Safety run-in phase I : Safety and recommended dose for phase II trial during the Dose-limiting toxicities monitoring period
時間枠:From Cycle 1 Day 1 of the first patient included to Cycle 3 Day 1 of the sixth patient included (each cycle is 21 days) (Safety and Tolerability)
The recommended dose for phase II trial (RP2D) of ubamatamab in combination with carboplatin-paclitaxel + bevacizumab
From Cycle 1 Day 1 of the first patient included to Cycle 3 Day 1 of the sixth patient included (each cycle is 21 days) (Safety and Tolerability)
Efficacy phase II part
時間枠:1 month after Cycle 3 Day 1 of the sixth patient included (each cycle is 21 days).
Objective response rate (ORR): Percentage of patients experiencing complete (CR) or partial response (PR) as the best overall radiological response after 3 cycles of ubamatamab in combination with carboplatin-paclitaxel-bevacizumab based on RECIST 1.1 criteria
1 month after Cycle 3 Day 1 of the sixth patient included (each cycle is 21 days).

二次結果の測定

結果測定
メジャーの説明
時間枠
Safety during the whole treatment period
時間枠:From study treatment start to 90 days after the last dose of ubamatamab
Incidence of Treatment emergent Adverse events according to NCI CTCAE version 6.0 during the whole treatment period (Safety and Tolerability)
From study treatment start to 90 days after the last dose of ubamatamab
Objective response rate (ORR)
時間枠:Through study treatment completion, an average of 15 months.
Percentage of patients experiencing complete (CR) or partial response (PR) as the best overall radiological response during the whole study treatment period based on RECIST 1.1 criteria.
Through study treatment completion, an average of 15 months.
Duration of response in patients experiencing an objective response
時間枠:From study treatment start to disease progression or death whichever occurs first assessed up to 48 months.
Time from first objective response to first objective documented disease progression (based on RECIST v1.1 criteria), or to death (regardless of the cause in the absence of disease progression).
From study treatment start to disease progression or death whichever occurs first assessed up to 48 months.
Disease control rate (DCR)
時間枠:From study treatment start to end of treatment, an average of 15 months.
Percentage of patients experiencing complete (CR) or partial response (PR) or stable disease (SD) as the best overall radiological response during the whole treatment period based on RECIST 1.1 criteria.
From study treatment start to end of treatment, an average of 15 months.
Percentage of patients operated with late cytoreductive surgery
時間枠:After 3 cycles of treatment (each cycle is 21 days).

To determine the percentage of patients operated with late cytoreductive surgery (after 3 cycles of the study regimen), and among them the percentage of patients operated with complete surgery without any macroscopic residual lesion.

Patients who have not progressed or died at the time of analysis will be censored at the time of the latest date of assessment from their last evaluable RECIST assessment.

After 3 cycles of treatment (each cycle is 21 days).
Progression-free survival (PFS)
時間枠:From study treatment start to disease progression or death whichever occurs first assessed up to 48 months.
Time from treatment start until the date of event defined as the first objective documented disease progression (based on RECIST v1.1 criteria) or death (regardless of the cause in the absence of progression).
From study treatment start to disease progression or death whichever occurs first assessed up to 48 months.
Overall survival (OS)
時間枠:From study treatment start to death or end of study whichever occurs first assessed up to 48 months.
Time from the date from treatment start until death regardless of the cause. Any patient not known to have died at the time of analysis will be censored based on the last recorded date on which the patient was known to be alive.
From study treatment start to death or end of study whichever occurs first assessed up to 48 months.
Progression-free survival during subsequent line of treatment (PFS-ST)
時間枠:From new treatment start to progression or death whichever occurs first assessed up to 48 months.
Time from the start of the subsequent line of treatment until the date of event defined as the first objective documented progression (based on RECIST v1.1), or death (regardless of the cause in the absence of progression).
From new treatment start to progression or death whichever occurs first assessed up to 48 months.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Benoit YOU、HCL - Centre Hospitalier Lyon Sud

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2028年9月1日

研究の完了 (推定)

2030年4月1日

試験登録日

最初に提出

2026年1月14日

QC基準を満たした最初の提出物

2026年6月4日

最初の投稿 (実際)

2026年6月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月10日

QC基準を満たした最後の更新が送信されました

2026年7月9日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

はい

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する