A Study of XZP-5955 Tablets in Patients With NTRK or ROS1 Fusion Positive Locally Advanced or Metastatic Solid Tumors

Locally Advanced or Metastatic Solid Tumors Clinical Trial

Official title:

The Safety Tolerability Pharmacokinetic Characteristics and Efficacy of XZP-5955 Tablets in Patients With NTRK or ROS1 Gene Fusion Locally Advanced or Metastatic Solid Tumors in a Single-arm Open-label Multi-center Phase I/II Clinical Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04996121
• Other study ID #: XZP-5955-1001
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: December 6, 2021
• Est. completion date: June 2027

Study information

• Verified date: August 2021
• Source: Xuanzhu Biopharmaceutical Co., Ltd.
• Contact: Jingjing Dong
• Phone: +86-13811667040
• Email: dongjingjing[@]xuanzhubio.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A phase I/II study to examine the safety, tolerability, pharmacokinetics and efficacy of XZP-5955 tablets in patients with advanced solid tumors harboring NTRK or ROS1 gene fusion

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 360
• Est. completion date: June 2027
• Est. primary completion date: September 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female subjects aged =18 years old;

2. Phase I dose escalation period: Histologically or cytologically confirmed diagnosis of locally advanced, or metastatic solid tumor, assessed by investigator that no standard therapy exists, or the tumor has relapsed, progressed or was nonresponsive to available therapies, or intolerance, or not suitable to standard therapy at current stage. Priority will be given to patients who have previously documented NTRK or ROS1 gene fusion confirmed by the central laboratory; Phase I dose expansion and Phase II: Histologically or cytologically confirmed diagnosis of locally advanced, or metastatic solid tumor, patients can provide a written report of pathological diagnosis of NTRK or ROS1 positive tested by qualified laboratory;

3. Phase I dose expansion cohort 1 and Phase II cohort 1: locally advanced, or metastatic solid tumor with NTRK gene fusion Phase I dose expansion cohort 2 and Phase II cohort 2: locally advanced, or metastatic NSCLC with ROS1 gene fusion that has progressed to crizotinib and other therapies or was intolerance to crizotinib Phase I dose expansion cohort 3: locally advanced, or metastatic NSCLC with ROS1 gene fusion who have not previously received crizotinib or other therapy.

4. phase I dose escalation: at least 1 measurable target lesion according to RECIST version 1.1 Phase I dose expansion and Phase II: at least 1 measurable target lesion according to RECIST version 1.1 (Tumor lesions treated with prior radiation or other local treatment are considered measurable if they show definite progression)

5. ECOG PS 0-1

6. Life expectancy = 3 months.

7. Adequate organ function:

Baseline laboratory values fulfilling the following requirements: Absolute neutrophils count (ANC) =1.5 × 109/L; Platelets (PLTs) =75 × 109/L; Hemoglobin = 85g/L; Serum creatinine= 1.5 × ULN, or creatinine clearance =50 mL/min/1.73m2(only when serum creatinine>1.5 × ULN); Total serum bilirubin =1.5 × ULN; Liver transaminases (AST/ALT) = 2.5 × ULN,=3× ULN if liver metastases are present or liver cancer patients; Activated Partial Thromboplastin Time=1.5× ULN;International Normalized Ratio (INR)=1.5× ULN;

8. Eligible patients (male and female) who are fertile must agree to at least use a reliable contraceptive method with partner during the trial and within 90 days from the last dose; Women of childbearing age must have a negative serum pregnancy test within 7 days before the first dose of the trial.

Exclusion Criteria:

1. Received anti-tumor therapy such as chemotherapy, radiotherapy, biotherapy, endocrine therapy, immunotherapy or other therapy within 4 weeks prior to the first dose of the investigational drug except the following: Nitroso ureas or mitomycin C within 6 weeks before the first dose of the drug; Oral fluorouracil and small molecule targeted drugs within 2 weeks prior to the first dose of drug or within 5 half life (whichever is longer);

2. Received other unmarketed investigational drugs or treatments within 4 weeks prior to the first dose of the investigational drug;

3. Major organ surgery (except biopsy) or significant trauma within 4 weeks prior to first dose of the investigational drug or required elective surgery during the trial;

4. Adverse reactions to previous antitumor therapy have not recovered to NCI CTCAE 5.0 = grade 1 (except for alopecia, grade 2 peripheral neurotoxicity, stable hypothyroidism after hormone replacement therapy, etc.);

5. Inability to swallow drug, or a condition that the investigator judged to severely affect gastrointestinal absorption (eg:Chronic Diarrhea, intestinal obstruction, etc.);

6. Cerebral or meningeal metastases with clinical symptoms. The below patients were allowed to be included: those who were asymptomatic, stable, and did not require steroid treatment for more than 4 weeks prior to the start of study treatment (if the cerebral metastases had undergone radiotherapy or/and surgery, radiotherapy and surgery should be at least 1 month prior to the first dose) ;

7. Known active infections and currently need intravenous anti-infective therapy;

8. History of immune deficiencies, including positive HIV antibody tests;

9. Active Hepatitis B (HBsAg and/or HBcAb positive with HBV-DNA > 500IU/ml) or hepatitis c virus infection (positive test results of anti-HCV with positive HCV-RNA );

10. Known interstitial lung disease (except for radioactive pulmonary fibrosis that does not require steroid therapy);

11. History of serious cardiovascular disease;

12. Pregnant or lactating women.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Locally Advanced or Metastatic Non-small Cell Lung Cancer
• Locally Advanced or Metastatic Solid Tumors
• Neoplasms

Intervention

Drug:
• XZP-5955 tablets
Phase I dose escalation: For each dose cohort, XZP-5955 tablet will be administered orally, single dose for day 1 and then from day 4, administered for continuous cycles of 21 consecutive days for each cycle Phase I dose expansion: XZP-5955 tablet will be administered orally, once daily for continuous cycles of 21 consecutive days for each cycle. Some patients for PK sample collection, the drug will be administered single dose for day 1, then from day 4, administered for continuous cycles of 21 consecutive days for each cycle Phase II: XZP-5955 tablet will be administered orally, once daily for continuous cycles of 21 consecutive days for each cycle

Locations

Country	Name	City	State
China	Cancer Hospital Chinese Academy of Medical Sciences	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Xuanzhu Biopharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose (MTD) (Phase I dose escalation)	Determine MTD of XZP-5955	24days following first dose of XZP-5955
Primary	Number of patients with adverse events (Phase I dose escalation)	Incidence of AE as assessed by CTCAE 5.0	within 30 days from last dose
Primary	Overall Response Rate (ORR) by Blinded Independent Central Review (BICR) (Phase I dose expansion and phase II)	Per RECIST v1.1 as assessed by BICR	2 to 3 years after first dose of XZP-5955
Secondary	Phase I: Area under the concentration versus time curve of XZP-5955 in plasma (AUC)	To determine the area under the plasma concentration time curve (AUC) of XZP-5955	Pre-dose, up to 72h after drug on Day 1;pre-dose on day 8, day 15 of cycle 1, , pre-dose and up to 12h after drug on day21 of cycle 1;pre-dose on day1 of cycle 2 and 3
Secondary	Phase I: Maximum plasma concentration (Cmax) of XZP-5955	To determine the maximum plasma concentration (Cmax) of XZP-5955	Up to 72 hours post dose of Day 1
Secondary	Phase I: Oral clearance (CL/F) of XZP-5955	To determine the oral clearance (CL/F) of XZP-5955	Pre-dose, up to 72h after drug on Day 1;pre-dose on day 8, day 15 of cycle 1, pre-dose and up to 12h after drug on day21 of cycle 1;pre-dose on day1 of cycle 2 and 3
Secondary	objective response rate (ORR) (Phase I and Phase II)	To determine the preliminary objective response rate (ORR) by investigator	2 to 3 years after first dose of XZP-5955
Secondary	Progression free survival (PFS) (Phase I and Phase II)	To determine the PFS by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Duration of response (DOR) (Phase I and Phase II)	To determine the DOR by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Disease control rate (DCR) (Phase I and Phase II)	To determine the DOR by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Clinical benefit rate (CBR) (Phase I and Phase II)	To determine the CBR by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Time to response (TTR) (Phase I and Phase II)	To determine the TTR by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Death of response (DpR) (Phase I and Phase II)	To determine the DpR by BICR and investigator	2 to 3 years after first dose of XZP-5955
Secondary	Overall survival (OS) (Phase I expansion period and Phase II)	To determine the OS	2 to 3 years after first dose of XZP-5955
Secondary	Intracranial objective response rate (Phase I expansion period and Phase II)	2 to 3 years after first dose of XZP-5955	To determine the intracranial ORR
Secondary	Number of patients with adverse events ((Phase I dose expansion and Phase II)	Incidence of AE as assessed by CTCAE 5.0	within 30 days from last dose
Secondary	Pop PK of XZP-5955 and its metabolite (Phase II)	To determine the PopPK characteristics of XZP-5955	pre-dose, Tmax on Day1, pre-dose on day 8 of cycle 1, pre-dose on day 1 of Cycle 2, Tmax,ss on Day 1 of cycle 2, pre-dose on day 1 of cycle 3