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CTRI Number  CTRI/2022/07/044491 [Registered on: 29/07/2022] Trial Registered Prospectively
Last Modified On: 22/02/2024
Post Graduate Thesis  No 
Type of Trial  BA/BE 
Type of Study    
Study Design  Randomized, Crossover Trial 
Public Title of Study   Bioequivalence study of Capecitabine Tablets USP, 500 mg in adult human cancer patients under fed conditions. 
Scientific Title of Study
Modification(s)  
An open label, multicenter, balanced, randomized, two-treatment, four-period, two-sequence, full replicate crossover, single dose, pharmacokinetic bioequivalence study of Capecitabine Tablets USP, 500 mg of Novugen Oncology Sdn. Bhd. with Xeloda® (Capecitabine) 500 mg Film-Coated Tablets manufactured by Roche Pharma AG, Germany following single oral dose of 2000 mg (4 X 500 mg) in adult human cancer patients under fed conditions. 
Trial Acronym   
Secondary IDs if Any
Modification(s)  
Secondary ID  Identifier 
Amendment no. 3.1 dated: 03/Feb/2023  Protocol Number 
CBCC/2022/003 Version 2.0 dated:15/Apr/2022   Protocol Number 
CBCC/2022/003 Version 3.0 dated:01/Jul/2022  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sandeep Singh 
Designation  Vice President - Clinical Operations 
Affiliation  CBCC Global Research LLP 
Address  Second Floor, Skoda House, Opposite L J Campus, S G Highway, Sarkhej, Ahmedabad, Gujarat – 382210, India
Bodakdev
Ahmadabad
GUJARAT
382210
India 
Phone  9637555304  
Fax    
Email  sandeep.singh@cbccusa.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sandeep Singh 
Designation  Vice President - Clinical Operations 
Affiliation  CBCC Global Research LLP 
Address  Second Floor, Skoda House, Opposite L J Campus, S G Highway, Sarkhej, Ahmedabad, Gujarat – 382210, India
Bodakdev
Ahmadabad
GUJARAT
382210
India 
Phone  9637555304  
Fax    
Email  sandeep.singh@cbccusa.com  
 
Details of Contact Person
Public Query
 
Name  Dr Sandeep Singh 
Designation  Vice President - Clinical Operations 
Affiliation  CBCC Global Research LLP 
Address  Second Floor, Skoda House, Opposite L J Campus, S G Highway, Sarkhej, Ahmedabad, Gujarat – 382210, India
Bodakdev
Ahmadabad
GUJARAT
382210
India 
Phone  9637555304  
Fax    
Email  sandeep.singh@cbccusa.com  
 
Source of Monetary or Material Support
Modification(s)  
Novugen Oncology Sdn. Bhd., No. 3, Jalan Jururancang U1/21, Hicom Glenmarie Industrial Park, 40150 Shah Alam, Selangor, Malaysia  
 
Primary Sponsor
Modification(s)  
Name  Novugen Oncology Sdn Bhd 
Address  No. 3, Jalan Jururancang U1/21, Hicom Glenmarie Industrial Park, 40150 Shah Alam, Selangor, Malaysia  
Type of Sponsor  Pharmaceutical industry-Global 
 
Details of Secondary Sponsor  
Name  Address 
NA  NIL 
 
Countries of Recruitment     India  
Sites of Study
Modification(s)  
No of Sites = 9  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Minish Jain  CIMETs Inamdar Multispecality Hospital  Building S. No. 15, Behind KPCT Mall, Fatima Nagar, Pune-411040 Maharashtra, India
Pune
MAHARASHTRA 
9823133390

minishjain009@gmail.com 
Dr K Velavan   Erode Cancer Centre  1/393 Velavan Nagar, Perundurai Road, Thindal, Erode-638012, Tamil Nadu, India
Erode
TAMIL NADU 
9842334222

kvels@rediffmail.com 
Dr Rajnish Nagarkar  HCG Manavata Cancer Centre  Behind Shivang Auto, Mumbai Naka, Nashik, Maharashtra - 422002, India
Nashik
MAHARASHTRA 
9823061929

drraj@manavatacancercentre.com 
Dr Shanti Prakash Shrivastav  Kiran Multi Super Specialty Hospital  Near Sumul Dairy, Katargam, Surat, Gujarat 395004, India
Surat
GUJARAT 
9824196710

sp.shrivastav@kiranhospital.com 
Dr Mahesh Kalloli   KLES Dr. Prabhakar Kore Hospital and Medical Research Centre  Nehru Nagar, Belagavi, Karnataka-590010, India
Belgaum
KARNATAKA 
8312470400

Mahesh.kalloli@gmail.com 
Dr Aniket Thoke   Sanjeevani CBCC USA Cancer Centre, Raipur  front of Jain Mandir, Dawada Colony, Pachpedi Naka, Raipur, Chhattisgarh -492001, India
Raipur
CHHATTISGARH 
9752929741

drthoke@gmail.com 
Dr Honey Parekh  Sunshine Global Hospital  Dumas Road, Beside Big Bazar, Piplod, Surat, Gujarat - 395007, India
Surat
GUJARAT 
9977963162

honey18parekh@gmail.com 
Dr Deepak Kumar Singh  Swami Harshankaranand Ji Hospital and Research Center  N 8/237, BHU Road, Near Bhikaripur Crossing, Opposite Union Bank of India, B.H.U, Sundarpur, Newada, Varanasi,-221005, Uttar Pradesh, India
Varanasi
UTTAR PRADESH 
9450428608

deepakbhu@gmail.com 
Dr Rajiv Michael  Thanjavur Cancer Centre  165/16, By- pass Road, Madhakkottai, Thulukkampatti, Thanjavur-613005, Tamilnadu, India
Thanjavur
TAMIL NADU 
9597773959

rajivmrh@gmail.com 
 
Details of Ethics Committee
Modification(s)  
No of Ethics Committees= 9  
Name of Committee  Approval Status 
Ethics Committee Inamdar Multispeciality Hospital  Approved 
Independent EC, Namaste Integrated Services   Approved 
Institutional Ethics Committee Sunshine Global Hospital  Approved 
Institutional Ethics Committee Erode Cancer Center  Approved 
Institutional Ethics Committee Thanjavur Cancer Centre  Approved 
Institutional Ethics Committee, KLE University  Approved 
Institutional Ethics Committee, Sanjeevani Cancer Hospital   Approved 
Kiran Hospital Ethics Committee  Approved 
Manavata Clinical Research Institute Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Approved/Obtained 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: C801||Malignant (primary) neoplasm, unspecified,  
 
Intervention / Comparator Agent
Modification(s)  
Type  Name  Details 
Intervention  Capecitabine Tablets USP, 500 mg of Novugen Oncology Sdn. Bhd.   Dosage: single oral dose of 2000 mg (4 X 500 mg), Frequency: Once Daily, Route of Administration: Oral, Duration of Therapy: 4 Days.  
Comparator Agent  Xeloda (Capecitabine) 500 mg Film-Coated Tablets manufactured by Roche Pharma AG, Germany.  Dosage: single oral dose of 2000 mg (4 X 500 mg), Frequency: Once Daily, Route of Administration: Oral, Duration of Therapy: 4 Days.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  65.00 Year(s)
Gender  Both 
Details  Subjects will be considered eligible for the study based on the following criteria:
1. Willing and able to provide voluntary informed consent and able to comply with protocol requirements
2. Male or Female aged 18 to 65 years (both inclusive) having body mass index at least 17.00 calculated as weight in kg per height in m2.
3. Patients having Body Surface Area between 1.27 to 1.92 m2 (both inclusive) measured as per the Dubois formula.
4. Patients with histopathologically or cytologically confirmed colon or colorectal or breast cancer.
5. Patients with DukesC colon cancer who have undergone complete resection of the primary tumor and when treatment with fluoropyrimidine therapy alone is preferred. Or Patients with metastatic colorectal carcinoma in whom treatment with fluoropyrimidine therapy alone is preferred. Or Patients with locally advanced or metastatic breast cancer, after failure of taxanes and an anthracycline-containing chemotherapy regimen or for whom further anthracycline therapy is not indicated.
6. Patients requiring a daily dose of Capecitabine monotherapy and stabilized at least on one cycle of Capecitabine chemotherapy (ex.twice daily at a dose of 1250 mg per m2 for 2 weeks followed by one week rest period).
7. Cardiac ejection fraction Greater than or equal to 50Percentby echocardiogram at screening.
8. Eastern Cooperative Oncology Group (ECOG) performance status Lessthan or equal to2.
9. Acceptable hematology status:
a. Hemoglobin Greater than or equal to 9 g per dL
b. Absolute neutrophil count (ANC) Greater than or equal to 1500 cells per mm3
c. Platelet count Greater than or equal to 100,000 cells per mm3
d. WBC Greater than or equal to 3000 cells per mm3
10. Acceptable liver function:
a. Alanine aminotransferase (ALT) Lessthan or equal to2.5 X ULN
b. Aspartate aminotransferase (AST) Lessthan or equal to2.5 X ULN
c. Bilirubin Lessthan or equal to1.5 X ULN
d. Alkaline phosphatase Lessthan or equal to2.5 X ULN
11. Patients with creatinine clearance Greaterthan 60 mL pe rminute calculated as per Cockcroft and Gault Formula.
12. Patients with life expectancy of at least 3 months at the time of enrolment.
13. Non-smokers
14. Male patients must agree to use an effective method of contraception from screening, during treatment and for at least 3 months after the last dose of capecitabine.
15. Female patients with negative serum pregnancy test at screening and negative urine pregnancy test on Day 0.
16. Women of child bearing potential, (defined as women physiologically capable of becoming pregnant, unless they are using effective method of contraception during dosing of the investigational product) practicing two acceptable methods of contraception during treatment and for 6 months after the last dose of capecitabine.
Acceptable methods of contraception are
a. Oral or parenteral (injection) or patch or implant hormonal contraception which has been used continuously for at least one month prior to the first dose of study medication
b. Intrauterine device (IUD) or intrauterine system
c. Double barrier method of contraception (Condom and occlusive cap or condom and spermicidal agent)
d. Male sterilization (at least 6 months prior to the screening, should be the sole male partner for that patient)
e. Female sterilization (surgical bilateral oophorectomy) or tubal ligation within at least 6 weeks prior to study participation
f. Total abstinence partial abstinence is not acceptable.
17. No history of addiction to any recreational drug or drug dependence or alcohol addiction. 
 
ExclusionCriteria 
Details  Subjects will be excluded from the study based on the following criteria:

1. Known hypersensitivity or contraindication to fluoropyrimidine therapy or to any of the components of investigational product.
2. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption
3. Known central nervous system (CNS) metastasis.
4. Known deficiency of dihydropyrimidine dehydrogenase (DPD)
5. Patients with history of cardiac disease
6. Major surgical procedure (including periodontal) within 28 days of first dose of Investigational Product.
7. Surgical or other non-healing wounds.
8. Patients with major mucocutaneous and dermatological abnormality.
9. Patients with coagulopathy.
10. Patients with positive serology for Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), or Human Immunodeficiency Virus (HIV).
11. Patients with suspected signs and symptoms of COVID-19/confirmed novel coronavirus infection (COVID-19) or with a recent history (within 14 days) of travel/contact with any COVID-19 positive patient/isolation/quarantine.
12. Patients with positive urine screen for drugs of abuse.
13. Patients with positive urine alcohol test
14. History of other malignancies in the last 5 years (except in situ cancer or basal or squamous cell skin cancer).
15. Has not recovered to Grade 0 or 1 toxicity from previous anticancer treatments or previous investigational agents. Exceptions are alopecia (any grade is acceptable), haemoglobin Greater than or equal to 9.0 g/dL, fatigue (Grade 2 is acceptable), and peripheral neuropathy (stable Grade 2 is acceptable) (As per National Cancer Institute [NCI] Common Terminology Criteria for Adverse Events [CTCAE], V5.0)
16. Participation in any clinical study within 90 days prior to receiving the first dose of Investigational Product.
17. Loss of blood Greater than or equal 350 mL within 90 days prior to receiving the first dose of investigational product for the current study.
18. Patients taking or scheduled to receive any of the prohibited medications (as per appendix B)
19. Any other medical condition or uncontrolled systemic disease (e.g. cardiovascular disease, hypertension, diabetes mellitus etc.) that, in the opinion of the Investigator, may make it undesirable for the patient to participate in the study including but not limited to cirrhosis or psychiatric illness/social situations that would limit adherence to study requirements.
20. Lactating women.
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Centralized 
Blinding/Masking   Open Label 
Primary Outcome
Modification(s)  
Outcome  TimePoints 
To compare and evaluate bioequivalence of
Capecitabine Tablets USP, 500 mg of Novugen Oncology Sdn. Bhd. with Xeloda® (Capecitabine) 500 mg Film-Coated Tablets
manufactured by Roche Pharma AG, Germany,
following single oral dose of 2000 mg (4 X 500
mg) in adult human cancer patients under fed
conditions.
 
A total of 72 blood samples will be collected during the study at 00 Hr,00.17 hr,0.33,0.50,0.67,1.0,1.25,1.50,1.75,2.0,2.33,2.67,3.0,3.50,4.0,5.0,6.0,8.0 hrs 
 
Secondary Outcome  
Outcome  TimePoints 
To monitor the adverse events and to ensure the safety of patients.  A total of eighteen (18) blood samples of 3.0 mL each will be collected for PK analysis in each period of the study. A total of 72 blood samples will be collected during the study. 
 
Target Sample Size   Total Sample Size="40"
Sample Size from India="40" 
Final Enrollment numbers achieved (Total)= "40"
Final Enrollment numbers achieved (India)="40" 
Phase of Trial   N/A 
Date of First Enrollment (India)   05/08/2022 
Date of Study Completion (India) 07/10/2023 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="8"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   NONE 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary
Modification(s)  

This a An open label, multicenter, balanced, randomized, two-treatment, four-period, two-sequence, full replicate crossover, single dose, pharmacokinetic bioequivalence study of Capecitabine Tablets USP, 500 mg of Novugen Oncology Sdn. Bhd. with Xeloda® (Capecitabine) 500 mg Film-Coated Tablets manufactured by Roche Pharma AG, Germany following single oral dose of 2000 mg (4 X 500 mg) in adult human cancer patients under fed conditions.

 
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