CTRI/2024/09/074081 [Registered on: 19/09/2024] Trial Registered Prospectively
Last Modified On:
01/04/2025
Post Graduate Thesis
No
Type of Trial
Interventional
Type of Study
Drug
Study Design
Other
Public Title of Study
A Phase 1 Clinical Trial of AUR104 in Patients with Relapsed/Refractory Lymphoid Malignancies
Scientific Title of Study
A Phase 1, Open Label, Dose Escalation, Multicenter Study Evaluating the Safety, Pharmacokinetics, and Pharmacodynamics of Oral AUR104 in Patients with Select Relapsed/Refractory Lymphoid Malignancies (VIJAY-1)
Trial Acronym
VIJAY-1
Secondary IDs if Any
Secondary ID
Identifier
Protocol AUR104-101, Version 3.0, 04 Jan 2024
Protocol Number
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
Name
Dr Akhil Kumar
Designation
Chief Medical Officer, Clinical Development
Affiliation
Aurigene Oncology Limited
Address
39-40, KIADB Industrial Area, Phase II, Electronic City Hosur Road Bangalore
Bangalore KARNATAKA 560100 India
Phone
08071025444
Fax
Email
akhil_k@aurigene.com
Details of Contact Person Scientific Query
Name
Dr Sapan Kumar Behera
Designation
Senior Manager and Medical Lead, Clinical Development
Affiliation
Aurigene Oncology Limited
Address
39-40, KIADB Industrial Area, Phase II, Electronic City Hosur Road Bangalore
Bangalore KARNATAKA 560100 India
Phone
9438738896
Fax
Email
sapan_b@aurigene.com
Details of Contact Person Public Query
Name
Oduru Suresh Reddy
Designation
Clinical Project Manager
Affiliation
Aurigene Oncology Limited
Address
39-40, KIADB Industrial Area, Phase II, Electronic City Hosur Road Bangalore
Bangalore KARNATAKA 560100 India
Phone
9866225593
Fax
Email
suresh_o@aurigene.com
Source of Monetary or Material Support
Aurigene Oncology Limited, 39-40, KIADB Industrial Area Phase II Electronic City Hosur Road Bangalore 560100 Karnataka India.
Primary Sponsor
Name
Aurigene Oncology Limited
Address
39-40, KIADB Industrial Area, Phase II, Electronic City Hosur Road, Bangalore, Karnataka- 560100, India
Type of Sponsor
Pharmaceutical industry-Indian
Details of Secondary Sponsor
Name
Address
Aurigene Oncology Limited
39-40, KIADB Industrial Area, Phase II, Electronic City Hosur Road, Bangalore, Karnataka- 560100, India
6th Floor, Sahaj Icon, Near prime arcade, Anand Mahal Road, Adajan, Surat, Gujarat, India-395009. Surat GUJARAT
9969465723
anshul.oncology@gmail.com
Dr Ashutosh Panigrahi
All India Institute of Medical Sciences Bhubaneswar
Room no. 16, 1 Floor, Medical Oncology/ Haematology, AIIMS, Sijua, P/O Patrapada, Bhubaneswar, Odisha-751019, India Khordha ORISSA
9437147517
dr.ashupanigrahi@gmail.com
Dr Padmaja Lokireddy
Apollo Cancer Hospitals
Apollo Cancer Hospitals, Apollo Hospitals, Jubilee Hills, Hyderabad, Telangana – 500096, India. Hyderabad TELANGANA
9553077700
drloki2002@yahoo.com
Dr Siddhesh Kalantri
Chopda Medicare & research center Pvt. Ltd.
Magnum Heart Institute, 3/5, Patil Lane No. 1, Laxmi Nagar, Near K.B.H. Vidyalaya, Canada Corner, Nashik, Maharashtra- 422005, India. Nashik MAHARASHTRA
8437649501
sidkalantri@gmail.com
Dr Varun Bafna
Dr. Bafna’s Star Superspecialty Clinic and Hospital
Dr. Bafna’s Star Superspecialty Clinic and Hospital, Rukmini Nagar, E ward, Near LIC Ground, Kolhapur, Maharashtra – 416005, India
Kolhapur MAHARASHTRA
9066565353
drvarunbafna6@gmail.com
Dr Minish Mahendra Jain
Grant Medical Foundation Ruby Hall Clinic
40, Sassoon Road, Pune, Maharashtra – 411001, India Pune MAHARASHTRA
Kiran Multi Super Speciality Hospital & Research Centre
Second Floor, Clinical Research Department (beside blood bank area), Vasta Devdi Road, Near Sumul Dairy Road, Katargam, Surat, Gujarat -395004, India. Surat GUJARAT
9428638448
drpriyalrsavaliya@gmail.com
Dr Yogesh Anap
Kolhapur Cancer Centre Pvt. Ltd.
Third Floor Clinical Research Department, R.S.238, Opp. Mayur Petrol Pump, Gokul Shirgaon Kolhapur, Maharashtra, India - 416234 Kolhapur MAHARASHTRA
9867155930
yogesh.anap1@gmail.com
Dr Reshma Puranik
MMFHA Joshi Hospital
Clinical Research Department, 778, Shivajinagar, Opp. Kamala Nehru Park, Pune, Maharashtra- 411004, India. Pune MAHARASHTRA
9552544910
drpreshma@gmail.com
Dr Vinod Raosaheb Patil
Onco Life Cancer Centre Pvt Ltd
Talegaon General Hospital, Talegaon-Chakan Road, Yashwant Nagar, Talegaon Dabhade, Pune, Maharashtra -410506, India Pune MAHARASHTRA
9819865983
drvinodpatilolcccr@gmail.com
Dr Sudhir Kumar Atri
Pt. B.D. Sharma, Post Graduate Institute of Medical Sciences
Clinical Research Department, PGIMS, Rohtak, Haryana -124001 Rohtak HARYANA
9315895272
Ssmantri74@yahoo.com
Dr Shashikant Apte
Sahyadri Super Speciality Hospital
Nagar Road, Survey No. 185A, Shashtri Nagar, Near MSEB office Yerwada, Nagar Road, Pune, Maharashtra -411006, India Pune MAHARASHTRA
Institutional Ethics Committee Onco Life Cancer Centre
Approved
Institutional Ethics Committee Poona Medical Research Foundation
Approved
Institutional Ethics Committee Sunshine Global Hospital
Approved
Institutional Ethics Committee-Clinical Studies Apollo Hospitals Enterprise Limited
Approved
KCC Institutional Ethics Committee
Approved
Kiran Hospital Ethics Committee
Approved
Magna-care Ethics Committee
Approved
Sahyadri Hospitals Ltd. Ethics committee
Approved
Zenith Institutional Ethics Committee
Approved
Regulatory Clearance Status from DCGI
Status
Approved/Obtained
Health Condition / Problems Studied
Health Type
Condition
Patients
(1) ICD-10 Condition: C858||Other specified types of non-Hodgkin lymphoma,
Intervention / Comparator Agent
Type
Name
Details
Intervention
AUR104:5mg and 20mg Tablets
Once or Twice Daily approximately 6 cycles (ie.,168 days)
Comparator Agent
Not Applicable
Not Applicable
Inclusion Criteria
Age From
18.00 Year(s)
Age To
99.00 Year(s)
Gender
Both
Details
1) Males and females ≥ 18 years of age.
2) Eastern Cooperative Oncology Group (ECOG) Performance status of 0 or 1.
3) Acceptable bone marrow and organ function at screening as described below:
- ANC ≥ 1000/μL (without WBC growth factor support)
- Platelet count: For patients with CLL ≥ 50,000/μL, For patients with lymphomas ≥ 75,000/μL without bone marrow involvement and ≥ 50,000/μL with bone marrow involvement. These thresholds should be qualified without current transfusion support.
- Hemoglobin ≥ 9 g/dL (Transfusion is allowed to achieve this Hb).
- Total Bilirubin ≤ 1.5 x ULN (Patients with known Gilbert’s syndrome are allowed with a Total Bilirubin ≤ 2.5 x ULN).
- AST (SGOT) ≤ 3 x ULN (≤ 5 × ULN if known liver metastases).
- ALT (SGPT) ≤ 3 x ULN (≤ 5 × ULN if known liver metastases).
- Creatinine clearance (CrCl) ≥ 60 mL/min (either measured or estimated by the Cockcroft-Gault formula). Cockcroft-Gault formula for estimated creatinine clearance (eCrCl):(140 – Age) × Weight (kg) × (0.85 if Female)/(72 × serum creatinine in mg/dL).
4) Ability to swallow and retain oral medications.
5) Histopathological diagnosis of Non-Hodgkin Lymphoma (NHL) or Chronic Lymphocytic Leukemia (CLL) or Hodgkin disease.
Note:
5a. The lymphoma should be either in Stage III or IV according to Lugano classification at screening.
5b. The lymphomas included in this study must fall within one of the following 2017 World Health Organization categories except lymphoma mentioned in Exclusion criterion #5:
-Mature B-cell neoplasms (excluding plasma cell neoplasms, heavy chain disease, and primary central nervous system [CNS] lymphoma).
-Mature T- and NK-cell neoplasms.
-Hodgkin lymphomas.
5c. The CLL should be Binet Stage C/Rai stage III or IV, as per the International Workshop on Chronic Lymphocytic Leukemia (iwCLL) guidelines.
6) In the case of patients who have lymphoid malignancies for which high-dose chemotherapy and autologous stem cell transplantation (HD-ASCT) is considered standard curative therapy, eligibility for this study requires that the subject’s disease has relapsed after HD-ASCT, or the subject is not eligible for HD-ASCT, or the subject has refused HD-ASCT.
7) In the case of patients who have lymphoid malignancies for which CAR-T therapy is indicated, eligibility for this study requires that the disease has relapsed after CAR-T, or the patient is not eligible for CAR-T, or the patient has refused CAR-T, or the CAR-T is not available locally.
8) Evidence of measurable disease as per Lugano Criteria for Lymphoma or evidence of measurable disease as per iwCLL Criteria for CLL.
Note: Patients with Small Lymphocytic Lymphoma (SLL) alone or in combination with CLL are allowed.
9) Standard curative measures do not exist, and the patient must have exhausted all effective therapies available locally. At a minimum, the patients must have relapsed or refractory disease to at least 2 prior lines of systemic therapies for NHL or CLL, or Hodgkin’s disease.
Note: Any cancer patient with access to any effective therapy locally must not be enrolled.
ExclusionCriteria
Details
1) Systemic anti-cancer therapy, such as chemotherapy, biological therapy, or immunomodulatory drug therapy, received within the past 28 days or 5 half-lives, whichever is longer, from Cycle 1 Day 1 of the study.
Note: Concomitant use of low-dose prednisone (up to 10 mg/day) is allowed.
2) Presence of acute or chronic toxicity resulting from prior anti-cancer treatment, except for alopecia or nail changes that have not resolved to Grade ≤ 1, as determined by NCI CTCAE v 5.0.
3) Definitive Radiotherapy within the last 21 days of Cycle 1 Day 1 (limited field palliative radiation is allowed and no restrictions during the screening period or during the trial).
4) Use of any investigational agent within 28 days or 5 half-lives (whichever is longer) prior to Cycle 1 Day 1.
5) Patients with Burkitt’s lymphoma, Burkitt-like lymphoma, post-transplant lymphoproliferative disease, primary mediastinal large-B cell lymphoma, cutaneous lymphomas, mycosis fungoides (MF), or Sezary syndrome (SS).
6) Known symptomatic or untreated or recently treated (≤ 6 months of screening) central nervous system (CNS) lymphoma. Patients with previously treated (more than 6 months of screening) CNS lymphoma and are now stable and asymptomatic, from a CNS perspective, are allowed.
7) Patients with lymphoma requiring immediate cytoreductive therapy.
8) Patients with low-grade or indolent lymphoma not meeting conventional criteria for treatment.
9) Elevated Serum cardiac Troponin I or troponin T more than ULN at screening.
10) Serum magnesium and calcium levels more than 1.2 x ULN or less than 0.8x LLN.
11) Serum Potassium more than 1.0x ULN or less than 1.0x LLN.
Note: Patients experiencing hypokalemia are permitted to undergo treatment to attain normal potassium levels during the screening period.
12) Mean Heart Rate less than 60 at screening or Cycle 1 Day 1 (to be recorded at least 3 times at least 5 minutes apart) in ECG.
13) Left ventricular ejection fraction (LVEF) less than 50% as determined by an echocardiogram (ECHO) or Multigated Acquisition (MUGA) scan.
14) QTcF (Fridericia) interval more than 450 ms for patients on ECG at screening and/or at Cycle 1 Day 1.
15) Uncontrolled arterial hypertension defined as supine SBP of ≥ 140 mm Hg AND/OR supine DBP ≥ 90 mmHg on stable doses of three or lesser different classes of antihypertensive drugs.
Notes:
- Patients taking 4 or more classes of antihypertensives are excluded. Diuretics (such as furosemide or spironolactone) are considered as one class of anti-hypertensives.
- The blood pressure has to be recorded 3 times at least 10 minutes apart during Screening and Cycle 1 Day 1 (before dosing) in the supine position. Among these recordings, a single instance of SBP ≥140 mm Hg or DBP ≥ 90 mmHg will exclude the patient. Note: A patient excluded on these criteria can be re-screened after optimal BP management.
16) Current or past history of heart failure (NYHA Class 2 or higher)
17) Having a history of moderate to severe cardiovascular disease including unstable angina, myocardial infarction, cerebrovascular accident, or transient ischemic attack (TIA), within 1 year prior to Cycle 1 Day 1.
18) Ongoing cardiac arrhythmias or conduction blocks.
19) History of any ventricular arrhythmia including supraventricular or ventricular premature contractions.
20) Patients on drugs which are sensitive substrates of CYP3A4 and cannot be discontinued at least one week prior to Cycle 1 Day 1.
21) Use of strong CYP3A4 inhibitors or inducers within 2 weeks prior to Cycle 1 Day 1.
22) Concomitant use of any drug which is known to prolong QTc interval or use of such drugs within one week prior to Cycle 1 Day 1.
23) Major surgery ≤ 28 days from Cycle 1 Day 1 (major surgery is defined as a procedure requiring general anesthesia)
24) Active infection requiring systemic therapy.
Note: Prophylactic use of antibiotics is allowed. Any infection detected during the screening period, which is resolved adequately according to the investigator before Cycle 1 Day 1, is allowed.
25) Known to be human immunodeficiency virus (HIV) positive or have an acquired immunodeficiency syndrome-related illness.
26) Known active or chronic hepatitis B (HBsAg +ve) or hepatitis C infection (HCV antibody +ve).
27) Patient expected to require any other form of antineoplastic therapy or targeted therapy while in the study.
28) Uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, active peptic ulcer disease or significant gastritis, active bleeding diatheses, presence of any major medical illness (e.g., renal, hepatic, hematologic, gastrointestinal, endocrine, pulmonary, or psychiatric illness/social situations or clinically significant laboratory / ECG abnormalities at screening, any or a combination of illnesses, which, in the opinion of the PI, may either put the patient at risk because of participation in the study or influence the results or the patient’s ability to participate in the study
29) Current swab-positive or suspected (under investigation) Covid-19 infection or fever and other signs or symptoms suggestive of Covid-19 infection with recent contact of the person(s) with confirmed Covid-19 infection, at screening or Cycle 1 Day 1.
30) History of another primary malignancy within 5 years prior to starting the study drug, except for adequately treated basal or squamous cell carcinoma of the skin or cancer of the cervix in situ or cured early-stage (Stage 1 or 2) prostate cancer.
31) Positive pregnancy test for women of childbearing potential (WOCBP) at the screening or enrolment visit
32) Lactating women or WOCBP who are neither surgically sterilized nor willing to use reliable contraceptive methods (hormonal contraceptive, IUD, or any double combination of male or female condom, spermicidal gel, diaphragm, sponge, cervical cap).
Method of Generating Random Sequence
Other
Method of Concealment
Other
Blinding/Masking
Open Label
Primary Outcome
Outcome
TimePoints
Primary Endpoints
- First cycle DLT.
- Safety and tolerability of AUR104 as measured by NCI CTCAE v 5.0.
- PK parameters including but not limited to AUC(0-12), AUC (0-24), AUC0-t, Cmax, Cmin, Tmax, MRT, and t½.
28 days
Secondary Outcome
Outcome
TimePoints
Exploratory Endpoints
- PD biomarkers.
- Efficacy assessments of overall response rates (ORR), duration of response (DOR), Progression Free Survival (PFS), etc., as measured by Lugano Criteria for NHL/ Hodgkin lymphoma or iwCLL criteria for CLL.
PD biomarkers: 28 days
Efficacy: Baseline, Cycle 2, 4, 6, 9, 12 and then every 3 months thereafter
Target Sample Size
Total Sample Size="42" Sample Size from India="42" Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials" Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials"