A Clinical Study on Fasudil Hydrochloride for Treatment of Gene-Specific Ovarian Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorZhejiang Provincial People's Hospital

About this trial

This is a prospective study investigating whether the research on Fasudil Hydrochloride in the treatment of gene-specific ovarian cancer can be applied to predict sensitivity to immunotherapy in non-small cell lung cancer (NSCLC) and other tumors. The study plans to enroll 20 patients with A/A genotype ovarian cancer for treatment evaluation.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients voluntarily participate in the study, sign informed consent forms, and have good compliance.

After platinum based chemotherapy at Zhejiang Provincial People's Hospital, the efficacy evaluation showed that ovarian cancer patients who achieved disease stability (SD) or disease progression (PD) twice were treated with Fasudil in combination with the original chemotherapy regimen, and were confirmed to have the A/A genotype through genetic testing.

Disqualifiers

1.Accompanied by hypotension 2. Bleeding like cerebral hemorrhage 3. Patients with abnormal liver function

Trial design

Design model

Single group

Treatments tested in this trial

  • Fasudil Hydrochloride

    Drug

    Exploring whether the study of using Exploring whether the study of using Fasudil Hydrochloride for the treatment of gene specific ovarian cancer can be used to predict the sensitivity of immunotherapy for non-small cell lung cancer and other tumors for the treatment of gene specific ovarian cancer can be used to predict the sensitivity of immunotherapy for non-small cell lung cancer and other tumors

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Experimental: Fasudil HydrochlorideExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

ORR

Overall objective tumor response rate

Time frame
3 years

Secondary outcomes

1

PFS

Progression free Survial

Time frame
3 years

Other outcomes

Sponsors and contacts

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