ADAD forum webinar May 2012


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ADAD forum webinar May 2012

  1. 1. The DIAN Treatment Trials: An Update Sunday, May 6 4:00-5:00 PM CDT Presented by Randall Bateman, MD DIAN Therapeutic Trials Unit Director DIAN Clinical Core Leader
  2. 2. AgendaI. IntroductionsII. DIAN UpdateIII. DIAN Trials update a. Expanded Registry b. Therapeutic Trials TopicsIV. Q & A
  3. 3. The Dominantly Inherited Alzheimer’s Network DIAN Coordinating Center Cores Admin – JC Morris Genetics – AM Goate Clinical – RJ Bateman Imaging – T Benzinger Biomarkers – AM Fagan Informatics – D Marcus Biostatistics – C Xiong Neuropathology – NJ Cairns Performance Sites• United States: Washington Univ (Bateman), MGH/BWH (Sperling), Butler Hosp/Brown Univ (Salloway), Columbia Univ (Mayeux), Indiana Univ (Ghetti), UCLA (Ringman), U of Pittsburgh (Klunk), Mayo Clinic, Jacksonville (Graff-Radford)• Europe: Institute of Neurology, Univ College London (Rossor), Ludwig-Maximilians- Universität München (Danek), University of Tübingen (Jucker)• Australia: Prince of Wales Medical Research Institutes, Sydney (Schofield), Mental Health Health Research Institute, Melbourne (Masters), Edith Cowan Univ , Perth (Martins)f Pittsburgh (Klunk), Mayo Clinic, Jacksonville (Graff-Radford) Clinical Trials Committee DIAN family participant , Paul Aisen, Randy Bateman, Neil Buckholtz, Nick Fox, Alison Goate, Bill Klunk, Ranjit Mani, John Ringman, Laurie Ryan, Stephen Salloway, Reisa Sperling, Chengjie Xiong
  4. 4. DIAN Clinical Core Enrollment Report Initial Visits Follow-up Visits Follow-up Visits Actual In-Person Remote Year One (9/2008-6/2009) 11 0 0 Year Two (7/2009-6/2010) 76 0 5 Year Three (7/2010-6/2011) 103 25 40 Year Four(7/2011 through 2/2012) 52 34 60 YTD Totals 242 59 105
  5. 5. DIAN Therapeutic Trials Unit (TTU) Update• October, 2011: DIAN trials grant submitted to NIH.• December, 2011: DIAN Pharma Consortium formed (10 leading pharmaceutical companies) and TTU funded• 14 compounds nominated and reviewed: – anti amyloid-beta, passive immunotherapies, secretase inhibitors, others – 5 proposed for immediate consideration.• April, 2012: Expanded Registry launched
  6. 6. Pharma Consortium Members
  7. 7. DIAN Expanded Reaching out to Participants, Physicians And families
  8. 8. DIAN Expanded Registry• Provides an overview of Autosomal Dominant Alzheimer’s disease (ADAD), links to other web resources (• Operational as of Feb 2012, announced in April, ~65 interested participants have registered. – Current DIAN observational study participants, family members and those interested in future trials are registering on the website – Physicians and researchers interested in participating as an investigator or referring potential patients from their practice are also registering
  9. 9. DIAN Expanded Registry
  10. 10. DIAN Clinical Trials NIA Grant OverviewTitle: Dominantly Inherited Alzheimer Network Trials: An Opportunity to Prevent Dementia .Application submitted October 5, 2011, reviewed March 2, 2011Summary: The application proposes to initiate DIAN clinical trials with a two-phase study todelay, prevent, or restore cognitive loss in AD mutation carriers.The first phase to determine the biological engagement of the drug target and impact onbiomarkers of neurodegeneration.The second phase to determine if there is a cognitive benefit of treatment.
  11. 11. Grant Review Summary Statement“There was much enthusiasm for this innovativeapplication and its efficient linking with DIAN. The overallgoal of prevention for those patients at very high risk ofAD in this cohort is highly significant. The innovativedesign, strong investigative team and environment andthe compelling pilot data from the parent DIANparticipants are other big strengths of the proposedstudy.”Concern: Ability to recruit sufficient numbers ofparticipants (only counting numbers enrolled)
  12. 12. Trial Design Outline – Years 1 & 2• 3 parallel, placebo controlled, double-blinded, biomarker outcome trials• Up to 80 participants enrolled in each trial – 40 mutation carriers (30 on active drug treatment, 10 on placebo) – 10 to 40 non-carriers on placebo to maintain genetic status blind• Drug treatment duration = 2 years• Placebo participants pooled from the trials to provide a common pool of 30 placebo for comparison of biomarker (phase IIb) outcomes.
  13. 13. Trial Design Outline Years 3-5Outcomes:• If one trial is successful, it will continue while enrolling a total of 240 participants• If none of the three original trials is successful, and three new drugs are suitable and available, start 3 new biomarker trials.A B CDIAN study 3:1 active to Drug A, B, or C Years Years placebo monthly for 22 mo 0 1 2 3 4 5 0 1 2 3 4 5 (run-in) (pooled placebo) A (80) A (80) D (80) B (80) B (240) B (80) E (80) Biomarker, clinical, and cognitive measures and samples C (80) C (80) F (80)Figure 1. Trial Design and Potential Outcomes. 240 participants are enrolled into a four arm study of drug A,drug B, drug C, and placebo. Mutation negative participants are assigned placebo, while mutation positiveparticipants are randomized to drug or placebo in a 3:1 ratio (A). 80 participants will be enrolled in each ofthree two-year biomarker trials; 40 mutation carriers and up to 40 non-carriers will be enrolled in each trial.Biomarker outcomes through week 96 will be assessed before the start of Year 3. In B, one trial is successfuland continues while enrolling a total of 240 participants in the three-year cognitive endpoint trial. In C, noneof the three original trials is successful, and three new two-year biomarker trials are begun.
  14. 14. Clinical Trial Design• Study visits: – Monthly infusions or injections – Safety MRI every 3 months – Length of commitment is 2 years for first part of study, 3 additional years if a treatment is successful
  15. 15. Schedule of Events VISIT SITE DIAN DIAN Sat Sat Sat Sat Sat Sat Sat Sat Sat Sat Sat DIANPROCEDURE: Visit No V1 V2 V3 V4 V5 V6 V7 V8 V9 V10 V11 V12 V13 V14 Timing (wks.) -4 to 0 0 4 8 12 16 20 24 28 32 36 40 44 48 Informed consent X Medical/Treatment History X X X X X X X X X X X X X X Clinical Assessment X X Physical/Neurological Exam X X Vital signs X X X X X X X X X X X X X X 12- lead ECG X X X Questionnaire(s) X X X X XHematology/Chemistry/LFTs/UA X X X X X X Pregnancy testing (dipstick) X X X X X X X X X X X X X X Study Therapy Administration X X X X X X X X X X X X X Cognitive Testing X ? X PET-PIB X X F-18 PET X X Safety MRI X X X Volumetric MRI X X Lumbar Puncture (CSF) X X FDG-PET X X DIAN = DIAN observational study site location Sat = Satellite site
  16. 16. Inclusion/Exclusion• -15 before to +10 years after parental age of onset• Possible symptomatic or mild dementia eligible• Greater than 18 years of age• Non-carriers who know their mutation status are not eligible
  17. 17. Genetic Testing• DIAN can pay for discovery testing for appropriate families or DIAN participants.• DIAN can pay for Genetic Counseling and Testing.• DIAN Coordinators will assist in finding a genetic counselor in participant’s own area.• DIAN Coordinator will arrange payment with the associated billing office.
  18. 18. Trial Design Key Points• Run-in design using DIAN data – Need consistent DIAN follow-up visits• DIAN participants will have the first opportunity to enroll in the trials. DIAN participants will be taken first as they have baseline data collected – Others will be welcomed but may need to do DIAN baseline measurements• 75% chance of receiving active drug (25% chance of placebo)
  19. 19. Patient Randomization ChartBrief review and consenting to hearmore details about the study andpossible drug you may receive Full, detailed review of the study procedures, office visits, drug therapies (sign consent) Assigned to drug treatment or placebo (blinded to you and the physician). Begin 22 months of drug therapy.
  20. 20. DIAN Trials Grant ResubmissionReviewers’ concern: Ability to recruitsufficient numbers of participantsActions to address concerns• Show proof of participant numbers and interest in trials – Expanded registry – Site Expansion – Input from participants (letters of support, survey)
  21. 21. DIAN Trials Participant Status 242* Total Participants Enrolled (N=estimated based on %) % Mutation Carriers 63% (N=152) % eligible for trials 69% (N=105) Age-range: 15 years before - 10 years after Note: Goal is 120 the Parental Age at Onset CDR = 0 46% (N=48) CDR = 0.5 (prodromal) 36% (N=38) CDR => 1.0 (dementia) 18% (N=19) Numbers in parentheses are estimated based on percentage enrolled in DIAN
  22. 22. DIAN Trials Next Steps• DIAN Trials Start-Up: now through end of year – Grant resubmission: July 5th , 2012 – Protocol design (currently underway): statistical analysis; participant procedure/assessments selection; final therapy selection – FDA Meeting (late summer): meet with the FDA for their input and approval to proceed with the planned trial protocol – Site identification (currently underway): identification of sites with capabilities, experience, and training in performing trials in this patient population (neurologists) – Training of all sites (physicians and nurse coordinators) for the trial
  23. 23. DIAN Trials Next Steps• DIAN Trials Start-Up: continued – Ethics / IRB approval at each location (several months): review board to ensure trial is ethical and there are no patient safety issues; review informed consent document – Participant enrollment into the trial: end of year through next year – Participants undergo therapy administration and procedures to measure the effect of the therapy
  24. 24. Q & A Session
  25. 25. Questions from Participants1. Will an individual’s stage of disease (mildly vs. greatly symptomatic) affect their eligibility or response to treatment.2. Do you know what drugs will be used?3. Do you know what the possible side effects are?4. How will the study be administered?
  26. 26. Questions continued…5. How frequent are the study visits?6. Are we able to have weekend treatments?7. How long would a person be in a trial?8. If you know you have the mutation, would you be able to tell if the drug is working?9. When will the trials begin?
  27. 27. Questions continued…10.Will the participant continue taking their current medications (Namenda, Aricept, etc.) while on the trial drug?11.If not, how long before the trial drug is administered should the participant stop taking their medication?12.How is it decided which trial drug the participant is to receive?
  28. 28. Questions continued…13.What side effects of the trial drug should we (caretakers) be aware of and expect?14.Due to DIAN site locations vs. participant locations, have you been able to work out a system to have participant’s doctor administer the trial drug?