- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07736612
A Pan-RAS Inhibitor in Combination With Anti-Tumor Therapy in Participants With Advanced Pancreatic Cancer
26. august 2026 oppdatert av: 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.
Studieoversikt
Status
Har ikke rekruttert ennå
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
80
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Tingbo Liang, MD.
- Telefonnummer: +86 19941463683
- E-post: liangtingbo@zju.edu.cn
Studer Kontakt Backup
- Navn: Yiwen Chen, MD.
- E-post: yiwenchen0705@126.com
Studiesteder
-
-
Zhejiang
-
Hangzhou, Zhejiang, Kina
- the First Affiliated Hospital, School of Medicine
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
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.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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).
|
|
Eksperimentell: 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).
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective Response Rate
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Disease Control Rate (DCR)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: From enrollment to upto 2 years
|
Safety evaluation was done continuously during treatment by using CTCAE 5.0
|
From enrollment to upto 2 years
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
15. august 2026
Primær fullføring (Antatt)
30. august 2028
Studiet fullført (Antatt)
30. desember 2029
Datoer for studieregistrering
Først innsendt
27. juli 2026
Først innsendt som oppfylte QC-kriteriene
27. juli 2026
Først lagt ut (Faktiske)
30. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
31. august 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
26. august 2026
Sist bekreftet
1. juli 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CAPT08
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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