A Clinical Study of ZL-85FA Tablets

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorChengdu Zenitar Biomedical Technology Co., Ltd

About this trial

An open-label, multicenter phase I/IIa clinical study evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of ZL-85FA tablets in treating advanced solid tumors

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

1.It is known that there is severe allergy to the investigational drug or any of its excipients (lactose, microcrystalline cellulose, low substituted hydroxypropyl cellulose, glyceryl behenate, hydroxypropyl methylcellulose, film coated premix (gastric soluble)); 2.Currently or previously suffering from other malignant tumors (excluding fully treated basal cell carcinoma or squamous cell carcinoma, cervical carcinoma in situ), unless curative treatment has been carried out and there is evidence of no recurrence or metastasis within the past 5 years; 3.Symptomatic central nervous system (CNS) metastases or asymptomatic CNS metastases requiring steroid treatment within 2 weeks prior to the first use of the study drug. Subjects with malignant meningitis or leptomeningeal spread; 4.Have received the last systemic anti-tumor treatment (chemotherapy, targeted therapy, immunotherapy, biologics, etc.) within 4 weeks before the first administration, with mitomycin or nitrosamines within 6 weeks, and small molecule targeted drugs within 2 weeks before the first administration of the study drug or within 5 half lives of the known drug (whichever is longer); Local palliative radiotherapy within 2 weeks prior to the first use of the study drug; The last administration of endocrine therapy is within 2 weeks before the first administration of the investigational drug (excluding necessary drug castration treatment for patients with metastatic castration resistant prostate cancer); Chinese herbal medicine or traditional Chinese patent medicines and simple preparations with anti-tumor indications were received within 2 weeks before the first administration of the study drug; 5.Individuals with severe infections within 4 weeks prior to the first administration, or those with active infections requiring oral or intravenous antibiotic treatment within 2 weeks prior; Individuals with active pulmonary tuberculosis who have undergone sufficient treatment before their first medication and have stopped anti tuberculosis treatment for at least 3 months are eligible for enrollment; 6.Receive blood transfusion, recombinant human thrombopoietin, recombinant human interleukin-11, erythropoietin, granulocyte colony-stimulating factor and other treatments within 2 weeks before the first use of the investigational drug; 7.Patients who have received systemic corticosteroid (prednisone>10 mg/day or equivalent doses of similar drugs, continuously used for more than 4 days) or other immunosuppressive therapy within 14 days before the first administration; Excluding the following situations: treatment with topical, ocular, intra-articular, intranasal, and inhaled corticosteroids, and short-term prophylactic treatment with corticosteroids such as contrast agents.

Within 6 months prior to the first use of medication, there is a New York Heart Association (NYHA) grade II or higher congestive heart failure, unstable angina pectoris, myocardial infarction, or arrhythmia requiring treatment during screening, with a left ventricular ejection fraction (LVEF)<50%;

Primary cardiomyopathy (such as dilated cardiomyopathy, hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, restrictive cardiomyopathy, and undifferentiated cardiomyopathy);

Other cardiovascular and cerebrovascular diseases that have been determined by researchers to be unsuitable for inclusion.

Trial design

Design model

Sequential

Treatments tested in this trial

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 2.5mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 5mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 10mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 15mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 20mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 25mg, oral, once daily

  • ZL-85FA tablets

    Drug

    ZL-85FA tablets 30mg, oral, once daily

  • ZL-85FA tablets

    Drug

    Based on the results obtained from the dose escalation phase, the necessity and dosage of the IIa phase expansion cohort will be determined by the Drug Safety Review Committee (SMC) after discussion.

  • ZL-85FA tablets

    Drug

    Based on the results obtained from the dose escalation phase, the necessity and dosage of the IIa phase expansion cohort will be determined by the Drug Safety Review Committee (SMC) after discussion.

Treatment groups

51 Participants
are divided into 9 treatment groups

9

Treatment groups

See each treatment group below.

Group A: Dose escalation group 1Experimental treatment 1 intervention
Group B: Dose escalation group 2Experimental treatment 1 intervention
Group C: Dose escalation group 3Experimental treatment 1 intervention
Group D: Dose escalation group 4Experimental treatment 1 intervention
Group E: Dose escalation group 5Experimental treatment 1 intervention
Group F: Dose escalation group 6Experimental treatment 1 intervention
Group G: Dose escalation group 7Experimental treatment 1 intervention
Group H: Dose extension group 1Experimental treatment 1 intervention
Group I: Dose extension group 2Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Objective remission rate

defined as the proportion of subjects with an overall efficacy response of complete remission (CR) or partial remission (PR) after at least one post-baseline evaluation during the trial.

Time frame
Up to week 96

Secondary outcomes

1

Disease control rate

defined as the proportion of subjects with an overall efficacy response of CR, PR and stable disease (SD) after at least one post-baseline evaluation during the trial

Time frame
Up to week 96
2

Duration of response

defined as the duration from first remission (PR and CR) to disease progression or death

Time frame
Up to week 96
3

Progression free survival

defined as the time from first dose to disease progression or death

Time frame
Up to week 96
4

Overall survival

defined as the time from first dose to death

Time frame
Up to week 96

Other outcomes

Sponsors and contacts

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