PHARMACY AND POISONS ORDINANCE (Cap. 138) APPLICATION FOR A CLINICAL TRIAL/MEDICINAL TEST CERTIFICATE



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PHARMACY AND POISONS ORDINANCE (Cap. 138) APPLICATION FOR A CLINICAL TRIAL/MEDICINAL TEST CERTIFICATE PART A: TRIAL INFORMATION A1. Title of Clinical Trial (as stated in proposed Protocol) Protocol No. Protocol Date A2. Name of Applicant A3. Business Address of Applicant Tel. No. Fax No. A4. Name(s) of Principle Investigator(s) A5. Name(s) and Address of Institution(s) Conducting the trial A6. Is this a study for which a clinical trial certificate was issued previously but has expired / will soon expire? Yes, (CTC No. and date of expiry ) No A7. Is this study also the subject of an application for approval by the State Food and Drug Administration (SFDA)? Yes, (if available, the number of Drug Clinical Trial Approval Document( 藥 物 臨 床 研 究 批 件 號 ) _and the date of approval ) No CT Application form - English (Oct 2008) Pg 1 of 3

PART B: TRIAL DESCRIPTION B1. This study is single centre multi-centre B2. No. of study sites in H.K. Total no. of sites Site name(s) B3. Study sites outside Hong Kong (if any) No. of sites in each country (e.g. Mainland China 2 sites, Singapore 2 sites) B4. Type of Sponsorship Investigator initiated study Pharmaceutical company initiated study Name of sponsor: Address: B5. Recruitment Size Planned number of trial subjects in H.K. total planned number of trial subjects world-wide B6. Study Period Planned start date and planned end date B7. Phase of Clinical Trial to be conducted Phase I (First-In-Man? Yes No) Phase II Phase III Phase IV Describe if necessary: B8. The study is open label single blind double blind other (please specify) B9. The study is non-randomized randomized B10. Therapeutic area (e.g. Oncology, Endocrinology) B11. Disease type (e.g. NPC, DM) PART C: TRIAL DRUG(s) C1. Study drug(s) to be investigated C2. The study involves concurrent use of C3. Comparator drug(s) used (if any) C4. Concomitant drug(s) used (if any) placebo concomitant drug comparator drug not applicable (non of the above) CT Application form - English (Oct 2008) Pg 2 of 3

PART D: DECLARATION OF THE APPLICANT I /We* hereby declare that, if the application is approved and the trial proceeds: D1. Agree to submit local drug related safety reports, yearly progress reports, and the final study report of the clinical trial as stated in the attached Notice of requirement of local drug related safety reports, progress reports and final study report in clinical trial [Appendix 1]. D2. This study will be conducted in accordance with the Good Clinical Practice. D3. The information given in this application is true and correct. Signature Company stamp (if the applicant is a company) Signatory s name in block letters Date (DD/MM/YY) * Delete as appropriate PART E: FOR OFFICE USE ONLY Date Received Fee Paid CT Application form - English (Oct 2008) Pg 3 of 3

Appendix 1 DEPARTMENT OF HEALTH DRUG OFFICE DRUG REGISTRATION AND IMPORT/EXPORT CONTROL DIVISION Notice of requirement on reporting of local drug related safety report, progress report and final study report in clinical trial All certificate holders of clinical trial / medicinal test are required to report to this office the following: 1. All local drug-related safety reports i.e. reports on adverse drug reactions (ADRs). (a) (b) For adverse drug reactions that are both serious* and unexpected** as soon as possible. (The attached CIOMS form [Appendix 2] may be used for reporting.) (i) Fatal or life-threatening unexpected ADRs should be reported as soon as possible but no later than 7 calendar days after first knowledge by the sponsor that a case qualifies, followed by as complete a report as possible within 8 additional calendar days. This report must include an assessment of the importance and implication of the findings, including relevant previous experience with the same or similar medicinal products. (ii) Other serious, unexpected ADRs that are not fatal or life-threatening, it should be reported as soon as possible but no later than 15 calendar days after first knowledge by the sponsor that the case meets the minimum criteria for expedited reporting. For non-serious adverse reactions and serious adverse reactions that are expected, it should be reported in a brief summary at the conclusion of the trial. * Serious Adverse Drug Reaction or Adverse Event : A serious adverse event (experience) or reaction is any untoward medical occurrence that at any dose: results in death, is life-threatening, requires inpatient hospitalisation or prolongation of existing hospitalisation, results in persistent or significant disability/incapacity, or is a congenital anomaly/birth defect. Medical and scientific judgement should be exercised in deciding whether expedited reporting is appropriate in other situations, such as important medical events that may not be immediately life-threatening or result in death or hospitalisation but may jeopardize the patient or may require intervention to prevent one of the other outcomes listed in the definition above. These should also usually be considered serious. Examples of such events are intensive treatment in an emergency room or at home for allergic bronchospasm; blood dyscrasias or convulsions that do not result in hospitalisation; or development of drug dependency or drug abuse. ** Unexpected Adverse Drug Reaction: An adverse reaction, the nature or severity of which is not consistent with the applicable product information (e.g., Investigator s Brochure for an unapproved investigational medicinal product)

-2-2. Progress report on yearly basis and a final study report at the end of the study. The attached forms [Appendix 3 & 4 respectively] may be used for reporting. 3. Please forward all reports to the following address : Drug Registration and Import/Export Control Division Drug Office Department of Health 3/F Public Health Laboratory Centre, 382 Nam Cheong Street, Shek Kip Mei, Kowloon, Hong Kong (Fax: 2803-4962)

Appendix 2 CIOMS FORM SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS (first. last) 1a. COUNTRY 2. DATE OF BIRTH 2a. AGE Years 3. SEX 4-6 REACTION ONSET 8-12 CHECK ALL APPROPRIATE Day Month Year 7 + 13 DESCRIBE REACTION(S) (including relevant tests/lab date) Day Month Year TO ADVERSE REACTION PATIENT DIED INVOLVED OR PROLONGED INPATIENT HOSPITALISATION INVOLVED PERSISTENCE OR SIGNIFICANT DISABILITY OR INCAPACITY LIFE THREATENING CONGENITAL ANOMALY II. SUSPECT DRUG(S) INFORMATION 14. SUSPECT DRUG(S) (include generic name) 20. DID REACTION ABATE AFTER STOPPING DRUG? YES NO NA 15. DAILY DOSE(S) 16. ROUTE(S) OF ADMINISTRATION 21. DID REACTION 17. INDICATION(S) FOR USE 18. THERAPY DATES (from/to) 19. THERAPY DURATION III. CONCOMITANT DRUG(S) AND HISTORY 22. CONCOMITANT DRUG(S) AND DATES OF ADMINISTRATION (exclude those used to treat reaction) REAPPEAR AFTER REINTRO- DUCTION? YES NO NA 23. OTHER RELEVANT HISTORY (e.g. diagnostics, allergics, pregnancy with last month of period. etc.) IV. MANUFACTURER INFORMATION 24a. NAME AND ADDRESS OF MANUFACTURER 24b. MFR CONTROL NO. 24c. DATE RECEIVED BY MANUFACTURER DATE OF THIS REPORT 24d. REPORT SOURCE STUDY LITERATURE HEALTH PROFESSIONAL 25a. REPORT TYPE INITIAL FOLLOWUP

Appendix 3 DEPARTMENT OF HEALTH DRUG OFFICE DRUG REGISTRATION AND IMPORT/EXPORT CONTROL DIVISION Clinical Trial Yearly Progress Report Report period to CT cert no. Protocol No.: Protocol Title: Date of this report Start date: Anticipated end date: Target no. of patient (as stated in protocol) No of patient intend to recruit (per site) No of patient recruited (per site) No. of patient completed the trial (per site) No. of patient drop-out from study (per site) Reasons for drop-out: Any changes for principle investigator? (If yes please give details) Summary of amendments during report period (if any) Summary of serious Adverse Events (if any) Does SAE affect the study? How and what action has been taken Summary of complaints about the study (if any) Summary of recent findings (especially information about risks associated with the research ) Progress of study: According to Plan extend study period (reason) Premature termination (reason ) Name: Posting: Signature: Date:

DEPARTMENT OF HEALTH DRUG OFFICE DRUG REGISTRATION AND IMPORT/EXPORT CONTROL DIVISION Appendix 4 Clinical Trial Final Report Report period to Date of this report CT cert no. Protocol No.: Protocol Title: Start date: End date: Target no. of patient (as stated in protocol) No of patient intend to recruit (per site) No of patient recruited (per site) No. of patient completed the trial (per site) No. of patient drop-out from study (per site) Reasons for drop-out: Summary of serious Adverse Events (if any) Does SAE affect the study? How and what action has been taken Summary of complaints about the study (if any) Study duration: According to Plan extended study period (reason) Premature termination (reason ) Summary of study outcome Name: Posting: Signature: Date: