1 / 26

Factive® (gemifloxacin) Proposed for the treatment of Acute Bacterial Sinusitis Oscient Pharmaceuticals, NDA 21-158/S-0

Factive® (gemifloxacin) Proposed for the treatment of Acute Bacterial Sinusitis Oscient Pharmaceuticals, NDA 21-158/S-006. Renata Albrecht, MD Director, Division of Special Pathogen and Transplant Products CDER. Outline . Proposed Indication Acute Bacterial Sinusitis (ABS)

steffie
Download Presentation

Factive® (gemifloxacin) Proposed for the treatment of Acute Bacterial Sinusitis Oscient Pharmaceuticals, NDA 21-158/S-0

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Factive® (gemifloxacin)Proposed for the treatment of Acute Bacterial SinusitisOscient Pharmaceuticals, NDA 21-158/S-006 Renata Albrecht, MD Director, Division of Special Pathogen and Transplant Products CDER

  2. Outline • Proposed Indication • Acute Bacterial Sinusitis (ABS) • Approved Indications • CAP and ABECB • Review of NDA 21-158/S-006 • Adequate and well controlled studies • Question(s) to committee

  3. Proposed Indication • “Acute Bacterial Sinusitis due to S. pneumoniae, H. influenzae, M. catarrhalis, S .aureus (methicillin susceptible strains only), K. pneumoniae and E. coli.” • The proposed dosage regimen is 320 mg qd PO for 5 days.

  4. Approved Indications • “Acute bacterial exacerbation of chronic bronchitis caused by Streptococcus pneumoniae, Haemophilus influenzae, Haemophilus parainfluenzae, or Moraxella catarrhalis.” • “Community-acquired pneumonia (of mild to moderate severity) caused by Streptococcus pneumoniae (including multi-drug resistant strains [MDRSP])*, Haemophilus influenzae, Moraxella catarrhalis, Mycoplasma pneumoniae, Chlamydia pneumoniae, or Klebsiella pneumoniae**”

  5. Gemifloxacin ABS Studies

  6. Four studies reviewed previously • Nonapproval letters: • 2000 (Studies #009, #010) 7 days • 2002 (Studies #186, #206) 5 days • “concluded gemifloxacin is effective in treating…acute bacterial sinusitis (ABS)” • Concern regarding cutaneous reactions • Conclusion that benefit did not outweigh risk for this indication

  7. How was efficacy demonstrated? • Active controlled, noninferiority designs • Ambulatory patients with baseline: • Signs and symptoms of sinusitis • Radiographic findings • (Some with bacteria from sinus tap culture) • Evaluate on Rx, end of Rx, and follow-up • Success defined as resolution of clinical and radiographic findings after treatment • Met conditions outlined in the protocols

  8. What were the safety concerns? • Cutaneous reactions • Primarily rash • Consistently more frequent in gemi arms than control (across indications) • Increased with duration of treatment • More common in < 40 yo vs > 40 yo • More common in women than men • Spectrum ranged from mild to severe

  9. Rash Rates by Treatment Duration, Age and Gender Percent reporting rash 0 5 10 15 20 25 3 5 7 10 14 3 5 7 10 14 Duration of Therapy (days)

  10. Approval vs Nonapproval Decisions (1) • CAP and ABECB: • Serious diseases, high morbidity/ mortality for CAP, risk of patient decompensation with ABECB. • In clinical trials most patients >40 yo, male >50%. • Despite higher incidence of rash with gemifloxacin, benefit judged to exceed risk • AC meeting 2003 recommended approval • Approval April 4, 2003

  11. Approval vs Nonapproval Decisions (2) • ABS not approved in 2000 (7 day regimen) and in 2002 (5 day regimen) • Potentially serious morbidity? • Most patients female in clinical trials, mean age ~ 40 years • Rash: 7 day regimen > 5 day > (comparators) • Despite conclusion that gemifloxacin was effective, the overall recommendation was that the indication not be approved because the risk of adverse events exceeded benefit for treatment of ABS

  12. ABS, February 2005 (1) • The Factive applications were submitted before 2003 AC on acute bacterial sinusitis • Agreed that judged by the pre-2003 parameters the drug was effective • Reiterated concerns that rash was more common with gemifloxacin, and requested large comparative safety study to demonstrate convincingly that the incidence of skin reactions, particularly serious skin reactions, was clinically acceptable and no greater than comparator.

  13. ABS, February 2005 (2) • Stated that did not grant MDRSP for ABS • “A placebo-controlled trial demonstrating efficacy in ABS secondary to MDRSP would be required.”

  14. Current SubmissionNDA 21-158/S-006 New efficacy application: Submitted November 2005 Accepted for review March 2006

  15. Review of ABS • FDA review involves examination of the information submitted for both efficacy and safety, and includes review of both new information and previously reviewed information in the application • Includes clinical study information and post-marketing information since approval in 2003

  16. Safety • Clinical trial data from 8119 patients who received gemifloxacin (including 6775 patients in initial NDA 21-158) • Clinical trial data from 5248 patients on comparator drugs (included in initial NDA 21-158) • Post marketing safety information • (Interim study reports submitted since June 2006)

  17. Efficacy • All three comparative ABS studies used non-inferiority trials design. • Since 2002, there have been a number of public meetings and workshops on use of noninferiority trials and necessity to justify noninferiority margin. • At October 2003 AC meeting on ABS committee recommended superiority trial designs for ABS since an appropriate noninferiority margin could not be determined from available published placebo-controlled studies.

  18. Noninferiority (similarity) trial design • Used for many infectious diseases trials. • Appropriate for diseases whose spontaneous resolution without antimicrobial treatment is low (e.g. bacterial meningitis, bacterial pneumonia) • So, if clinical success is reproducibly <50% in placebo arm and reproducibly >80% on antimicrobial, there is a 30% benefit of antimicrobial therapy. A margin of <30% for lower bound of 95% C.I. excludes that the effect may be due to placebo. Choosing a margin of <15% preserves at least half the benefit. • But, if clinical success is >70% in placebo arm (>80% for drug), the benefit is only <10%, and a much smaller margin must be selected to assure that the effect seen in the study is not due to placebo

  19. What is benefit of antimicrobial over placebo in ABS? • Review of published placebo-controlled studies in acute sinusitis • 17 articles published since 1964 • Eight published after 2000 (6 adult, 2 peds) • Why is this important? • Challenges in determining benefit of antimicrobial over placebo

  20. 21 CFR 314.126(b)(2)(iv) Adequate and Well Controlled studies • Active treatment concurrent control trials • “If the intent of the trial is to show similarity of the test and control drugs, the report of the study should assess the ability of the study to have detected a difference between treatments. Similarity…can mean either than both drugs were effective or that neither was effective. The analysis of the study should explain why the drugs should be considered effective in the study, for example, by reference to results in previous, placebo-controlled studies of the active control drug.”

  21. Laws and Regulations • Substantial evidence means… “evidence consisting of adequate and well-controlled investigations, including clinical investigations, by experts…, on the basis of which it could fairly and responsibly be concluded…that the drug will have the effect it purports or is represented to have …” • For approval, need “substantial evidence”

  22. Review of NDA 21-158/S-006 • Efficacy • Although Factive determined to be effective in ABS in 2000, 2002, the indication was turned down due to an unacceptable safety profile • As we examine efficacy in 2006, need to consider developments since 2002 • Safety • Concerns regarding ADR profile and signal in 2000, 2002 led to nonapproval • As we examine safety in 2006, need to consider safety data from clinical studies and post-marketing

  23. Today’s Agenda • Oscient Presentations • FDA presentations: • Update on sinusitis drug development (Dr. Powers) • Safety and efficacy of Factive for sinusitis (Dr. Tierney) • Post-marketing reports for gemifloxacin (Dr. Mosholder) • Open public hearing • Questions to the committee

  24. Question(s) to the Committee • Do the safety and effectiveness data presented demonstrate an acceptable risk/benefit profile for the use of Factive™ (gemifloxacin) as treatment of patients with acute bacterial sinusitis?

  25. Question(s) to the Committee • If yes, are there any special caveats, warnings or limitations that should be included in the label? Do you have any specific risk-management recommendations for Factive® (gemifloxacin) post approval? • If no, are there other studies or other information that could demonstrate that benefit outweighs the risk for this indication?

  26. Bob Temple Ed Cox Steve Gitterman Brenda Marques Leonard Sacks Maureen Tierney John Powers Igor Cerny Jayne Peterson Dornette Spell LeSane Sohail Mosaddegh Bob O’Neill Karen Higgins Cheryl Dixon Gerald Dal Pan Mark Avigan Rosemary Johann-Liang Andy Mosholder Evelyn Farinas OSE Staff DDMAC Compliance Thank You

More Related