- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07736612
A Pan-RAS Inhibitor in Combination With Anti-Tumor Therapy in Participants With Advanced Pancreatic Cancer
26 sierpnia 2026 zaktualizowane przez: TingBo Liang, Zhejiang University
A Phase Ib/II Study of the Safety, Tolerability, and Efficacy of a Pan-RAS Inhibitor in Combination With Anti-Tumor Therapy in Participants With Advanced Pancreatic Cancer
This study aims to evaluate the safety, tolerability, and efficacy of HRS-2329 in combination with other anti-tumor therapies in participants with advanced pancreatic cancer harboring RAS mutations or amplifications.
Przegląd badań
Status
Jeszcze nie rekrutacja
Interwencja / Leczenie
Typ studiów
Interwencyjne
Zapisy (Szacowany)
80
Faza
- Faza 2
- Faza 1
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Tingbo Liang, MD.
- Numer telefonu: +86 19941463683
- E-mail: liangtingbo@zju.edu.cn
Kopia zapasowa kontaktu do badania
- Nazwa: Yiwen Chen, MD.
- E-mail: yiwenchen0705@126.com
Lokalizacje studiów
-
-
Zhejiang
-
Hangzhou, Zhejiang, Chiny
- the First Affiliated Hospital, School of Medicine
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Nie
Opis
Inclusion Criteria:
- Age ≥ 18 years.
- Histopathologically confirmed locally advanced or metastatic pancreatic adenocarcinoma (originating from pancreatic ductal epithelium) that is not amenable to curative therapy.
- RAS mutation or amplification detected in tumor tissue or blood (by RAS testing).
Prior anti-tumor therapy:
- For cohort HRS-2329-A: at least one line of standard systemic therapy in the advanced setting;
- For cohorts HRS-2329-B and HRS-2329-C: at most one line of standard systemic therapy in the advanced setting.
- At least one measurable lesion according to RECIST version 1.1 criteria.
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1.
- Life expectancy ≥ 3 months.
- Adequate function of vital organs.
- Use of appropriate contraceptive methods during the study period, and so forth.
- Voluntary participation in this study with signed informed consent, good compliance, and willingness to cooperate with follow-up assessments.
Exclusion Criteria:
- Prior treatment with drugs similar to the investigational product.
- Known presence of central nervous system (CNS) metastases.
- Acute or chronic pancreatitis requiring clinical intervention.
- Gastrointestinal disorders that may affect drug administration/absorption, including but not limited to dysphagia, malabsorption syndrome, refractory nausea, vomiting, or diarrhea, Crohn's disease, and ulcerative colitis.
- Gastrointestinal obstruction, or signs/symptoms of gastrointestinal obstruction; however, patients who have undergone surgical intervention with complete resolution of the obstruction may be considered for screening.
- Concurrent biliary obstruction with risk of biliary tract infection (patients with treatable biliary obstruction may be enrolled if adequate biliary drainage is achieved and the risk of biliary infection is resolved after treatment).
- Third-space fluid collections (e.g., massive pleural effusion, ascites) that cannot be stabilised (i.e., no intervention required after drainage removal) within 2 weeks prior to enrolment; patients with only a small amount of fluid detected by imaging and without clinical symptoms may be enrolled.
- Severe infection within 4 weeks prior to enrolment, such as severe pneumonia, bacteraemia, or infectious complications requiring hospitalisation; unexplained fever >38.5°C within 2 weeks prior to enrolment ; signs/symptoms of infection requiring intravenous antibiotic therapy within 2 weeks prior to enrolment.
- Severe cardiovascular or cerebrovascular diseases.
- Known or suspected interstitial lung disease (isolated imaging findings of interstitial changes are not excluded).
- History of definite neurological or psychiatric disorders, including epilepsy and dementia.
- Non-healing wounds (severe, non-healing, or dehiscent), or unhealed fractures.
- Adverse events from prior therapy not recovered to NCI-CTCAE Grade ≤1 at enrolment .
- History of malignancies other than the primary tumour within 5 years prior to enrolment, with the exception of malignancies with low risk of metastasis and death, such as adequately treated carcinoma in situ of the cervix, basal cell carcinoma, or squamous cell carcinoma of the skin.
- Active hepatitis B infection.
- For Cohort C, conditions that are unsuitable for immunotherapy.
- Known allergy to any component of any of the study drugs to be administered.
- Any other condition that, in the investigator's judgement, may affect the study results or result in premature termination of the study.
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Zadanie sekwencyjne
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Arm A
This arm evaluates HRS-2329 in combination with nimotuzumab in participants with advanced pancreatic cancer harboring RAS mutations or amplifications who have received at least one prior line of therapy.
Approximately 6 to 10 participants are planned to be enrolled initially to assess safety and preliminary efficacy, at the prespecified dose of HRS-2329 plus nimotuzumab 400 mg (D1,D8,Q3W).
If the safety at this dose level is acceptable, enrollment may be expanded to 15-20 participants.
During this period, the Safety Monitoring Committee (SMC) may review the cumulative safety and efficacy data and, after discussion, decide whether to adjust the dose, add other dose groups or dosing frequency arms for further exploration, or discontinue this combination regimen.
|
Nimotuzumab is a marketed drug, a recombinant humanized monoclonal antibody targeting the epidermal growth factor receptor (EGFR).
Nimotuzumab is administered at 400 mg by intravenous infusion over at least 60 minutes on Days 1 and 8 of each 3-week cycle.
HRS-2329 is a novel, potent, oral pan-RAS inhibitor.
HRS-2329 is given orally (to be swallowed whole, not chewed).
It should be taken orally within 30 minutes after breakfast each morning.
|
|
Eksperymentalny: Arm B
This arm evaluates HRS-2329 and HS-20093 with or without nimotuzumab in participants with advanced pancreatic cancer harboring RAS mutations or amplifications who are treatment-naïve or have received up to one prior line of standard systemic therapy.
Approximately 30 participants are planned to be enrolled.
The prespecified doses are HRS-2329 plus HS-20093, with or without nimotuzumab 400 mg on Day 1 and Day 8 of each 3-week cycle.
The Safety Monitoring Committee (SMC) may review the cumulative safety and efficacy data and, after discussion, decide whether to adjust the dose, add other dose groups or dosing frequency arms for further exploration, or discontinue this combination regimen.
|
Nimotuzumab is a marketed drug, a recombinant humanized monoclonal antibody targeting the epidermal growth factor receptor (EGFR).
Nimotuzumab is administered at 400 mg by intravenous infusion over at least 60 minutes on Days 1 and 8 of each 3-week cycle.
HRS-2329 is a novel, potent, oral pan-RAS inhibitor.
HRS-2329 is given orally (to be swallowed whole, not chewed).
It should be taken orally within 30 minutes after breakfast each morning.
HS-20093 is a B7-H3 antibody-drug conjugate (ADC).
|
|
Eksperymentalny: Arm C
Alternative arm: This arm evaluates HRS-2329 and HS-20093 in combination with adebrelimab in participants with advanced pancreatic cancer harboring RAS mutations or amplifications who are treatment-naïve or have received up to one prior line of standard systemic therapy.
Approximately 30 participants are planned to be enrolled.
The prespecified doses are HRS-2329 plus HS-20093 plus adebrelimab 1200 mg Q3W.
The Safety Monitoring Committee (SMC) may review the cumulative safety and efficacy data and, after discussion, decide whether to adjust the dose, add other dose groups or dosing frequency arms for further exploration, or discontinue this combination regimen.
|
Adebrelimab is a recombinant humanized anti-PD-L1 monoclonal antibody injection.
It specifically blocks the binding of PD-1 to PD-L1, thereby terminating the immunosuppressive signals transmitted through PD-1 to T cells.
This enables T cells to re-recognize tumor cells and exert cytotoxic effects, ultimately inhibiting tumor growth.
Adebrelimab injection is administered at 1200 mg by intravenous infusion on Day 1 of each 3-week cycle.
HRS-2329 is a novel, potent, oral pan-RAS inhibitor.
HRS-2329 is given orally (to be swallowed whole, not chewed).
It should be taken orally within 30 minutes after breakfast each morning.
HS-20093 is a B7-H3 antibody-drug conjugate (ADC).
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Objective Response Rate
Ramy czasowe: From enrollment to upto 2 years
|
The proportion of patients whose tumor size shrinks as complete response or partial response, as assessed by RECIST1.1.
|
From enrollment to upto 2 years
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Disease Control Rate (DCR)
Ramy czasowe: From enrollment to upto 2 years
|
defined as the proportion of patients with advanced or metastatic cancer who have achieved a complete response (CR), partial response (PR), or stable disease (SD) as the best overall response, relative to the total number of evaluable patients.
|
From enrollment to upto 2 years
|
|
Duration of Response
Ramy czasowe: From enrollment to upto 2 years
|
defined as the time from the first documented objective response (Complete Response [CR] or Partial Response [PR]) to the first documented disease progression (per RECIST 1.1 criteria) or death due to any cause, whichever occurs first.
|
From enrollment to upto 2 years
|
|
Progression-Free Survival
Ramy czasowe: From enrollment to upto 2 years
|
defined as the time from initiation of treatment until the first documented disease progression per RECIST 1.1 criteria, or death due to any cause, whichever occurs first.
|
From enrollment to upto 2 years
|
|
Overall Survival
Ramy czasowe: From enrollment to upto 2 years
|
defined as the time from initiation of treatment until death from any cause.
|
From enrollment to upto 2 years
|
|
Adverse event
Ramy czasowe: From enrollment to upto 2 years
|
Safety evaluation was done continuously during treatment by using CTCAE 5.0
|
From enrollment to upto 2 years
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
15 sierpnia 2026
Zakończenie podstawowe (Szacowany)
30 sierpnia 2028
Ukończenie studiów (Szacowany)
30 grudnia 2029
Daty rejestracji na studia
Pierwszy przesłany
27 lipca 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
27 lipca 2026
Pierwszy wysłany (Rzeczywisty)
30 lipca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
31 sierpnia 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
26 sierpnia 2026
Ostatnia weryfikacja
1 lipca 2026
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- CAPT08
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIE
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .