RecruitingPhase IIIFemale onlyEN originalOvarian cancer

Torvutatug Samrotecan Plus Bevacizumab as First-line Maintenance in Homologous Recombination Deficiency (HRD) Negative Advanced Epithelial Ovarian Cancer

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This study will evaluate the efficacy, safety and tolerability of Torvutatug samrotecan (torvu-sam) in combination with bevacizumab compared with bevacizumab monotherapy as first line maintenance treatment in patients with Homologous Recombination Deficient (HRD) negative advanced ovarian cancer.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Pacjentki z nowo zdiagnozowanym zaawansowanym rakiem nabłonkowym jajnika, jajowodu lub otrzewnej (stopień III/IV wg FIGO), potwierdzonym histologicznie.
  • •Dostarczenie próbki guza z poprzednich badań (próbka utrwalona formaliną i zatopiona w parafinie).
  • •Pacjentki, które zakończyły od 6 do 8 cykli chemioterapii opartej na platynie jako pierwszym leczeniu, przed rozpoczęciem badania.
  • •Pacjentki, które otrzymały co najmniej 3 cykle Bevacizumabu w połączeniu z ostatnimi 3 cyklami chemioterapii przed rozpoczęciem badania.
  • •Pacjentki po operacji usunięcia guza lub z chorobą nieoperacyjną.
  • •Pacjentki z chorobą, która nie postępowała po zakończeniu wstępnego leczenia.
  • •Guzy pacjentek z niedoborem rekombinacji homoloogicznej (HRD-negatywne).

✗ Disqualifies

  • •Pacjentki z guzami nienabłonkowymi, guzami granicznymi lub guzami nabłonkowymi niskiego stopnia złośliwości.
  • •Pacjentki z historią choroby płuc (niezakaźne zapalenie płuc/śródmiąższowe choroby płuc) wymagającej leczenia sterydami lub dodatkowego tlenu, lub z obecnym zapaleniem płuc.
  • •Pacjentki z niezgojonymi ranami, aktywnymi owrzodzeniami lub złamaniami kości.
  • •Pacjentki z objawami niedrożności jelit.
  • •Pacjentki, które wcześniej przyjmowały terapie ukierunkowane na receptor FRα lub jakiekolwiek koniugaty lek-przeciwciało skierowane przeciwko TOP1.

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
October 1, 2026
Sex
Female only

Therapies / drugs in trial

Locations (186)

Research Site

Tampa, United States

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Baltimore, United States

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Billings, United States

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Cleveland, United States

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Buenos Aires, Argentina

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Buenos Aires, Argentina

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Capital Federal, Argentina

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Ciudad de Buenos Aires, Argentina

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Ciudad de Buenos Aires, Argentina

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Córdoba, Argentina

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Córdoba, Argentina

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Córdoba, Argentina

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Rosario, Argentina

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Salta, Argentina

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Santa Fe, Argentina

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Viedma, Argentina

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Auchenflower, Australia

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Benowa, Australia

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Hobart, Australia

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Kingswood, Australia

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Nedlands, Australia

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Port Macquarie, Australia

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Randwick, Australia

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Richmond, Australia

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Toorak Gardens, Australia

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Wollongong, Australia

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Fortaleza, Brazil

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Itajaí, Brazil

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Jaú, Brazil

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Natal, Brazil

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Porto Alegre, Brazil

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Rio de Janeiro, Brazil

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Salvador, Brazil

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São Paulo, Brazil

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São Paulo, Brazil

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São Paulo, Brazil

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Dobrich, Bulgaria

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Plovdiv, Bulgaria

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Shumen, Bulgaria

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Sofia, Bulgaria

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Sofia, Bulgaria

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Sofia, Bulgaria

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Toronto, Canada

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Montreal, Canada

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Santiago, Chile

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Santiago, Chile

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Temuco, Chile

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Viña del Mar, Chile

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Beijing, China

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Beijing, China

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Beijing, China

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Beijing, China

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Binzhou Shi, China

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Changchun, China

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Changsha, China

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Chengdu, China

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Chongqing, China

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Fuzhou, China

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Guangzhou, China

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Haikou, China

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Hangzhou, China

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Hangzhou, China

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Hangzhou, China

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Hefei, China

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Huangpu District, China

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Jinan, China

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Jinan, China

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Linyi, China

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Luzhou, China

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Nanchang, China

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Nanjing, China

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Nanjing, China

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Neijiang, China

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Shanghai, China

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Shanghai, China

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Shenzhen, China

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Shijiazhuang, China

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Suzhou, China

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Taiyuan, China

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Weifang, China

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Wenzhou, China

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Wuhan, China

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Xinxiang, China

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Xuzhou, China

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Bogotá, Colombia

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Bogotá, Colombia

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Medellín, Colombia

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Pasto, Colombia

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Berlin, Germany

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Bonn, Germany

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Hanover, Germany

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Wiesbaden, Germany

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Athens, Greece

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Pátrai, Greece

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Ansārinagar, India

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Bhubaneswar, India

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Hyderabad, India

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Mumbai, India

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Mumbai, India

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Nagpur, India

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Nashik, India

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New Delhi, India

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Pune, India

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Thiruvananthapuram, India

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Hadera, Israel

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Haifa, Israel

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Haifa, Israel

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Holon, Israel

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Jerusalem, Israel

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Kfar Saba, Israel

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Nahariya, Israel

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Tel Aviv, Israel

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Florence, Italy

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Genova, Italy

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Fukushima, Japan

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Ginowan-shi, Japan

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Hidaka-shi, Japan

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Isehara-shi, Japan

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Kashiwa-shi, Japan

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Kawasaki-shi, Japan

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Kobe, Japan

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Kōtoku, Japan

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Kurume-shi, Japan

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Kyoto, Japan

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Minatoku, Japan

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Nagoya, Japan

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Nagoya, Japan

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Niigata, Japan

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Osaka, Japan

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Osaka, Japan

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Ota-shi, Japan

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Sagamihara-shi, Japan

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Sapporo, Japan

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Sapporo, Japan

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Sendai, Japan

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Shinjuku-ku, Japan

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Shiwa-gun, Japan

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Suita, Japan

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Sunto-gun, Japan

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Toon-Shi, Japan

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Tsu, Japan

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Yokohama, Japan

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Yokohama, Japan

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Kuala Lumpur, Malaysia

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Kuala Selangor, Malaysia

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Kuala Selangor, Malaysia

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Petaling Jaya, Malaysia

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Arequipa, Peru

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Lima, Peru

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Lima, Peru

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Lima, Peru

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Wanchac, Peru

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Cebu, Philippines

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City of Muntinlupa, Philippines

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Quezon, Philippines

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Trenčín, Slovakia

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Ljubljana, Slovenia

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Busan, South Korea

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Daegu, South Korea

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Goyang-si, South Korea

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Gyeonggi-do, South Korea

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Seongnam-si, South Korea

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Seoul, South Korea

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Seoul, South Korea

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Seoul, South Korea

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Seoul, South Korea

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Seoul, South Korea

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Seoul, South Korea

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Yangsan, South Korea

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Barcelona, Spain

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Barcelona, Spain

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Kaohsiung City, Taiwan

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Kaohsiung City, Taiwan

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New Taipei City, Taiwan

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Taichung, Taiwan

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Taichung, Taiwan

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Tainan, Taiwan

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Tainan, Taiwan

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Taipei, Taiwan

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Taipei, Taiwan

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Taipei, Taiwan

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Taipei, Taiwan

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Taoyuan, Taiwan

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Bangkok, Thailand

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Bangkok, Thailand

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Bangkok, Thailand

Trial contact

AstraZeneca Clinical Study Information Center

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 10/2/2026.

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