Zolgensma Approval and Access June 2019 After Approval - Access 1. - - PowerPoint PPT Presentation

zolgensma approval and access june 2019 after approval
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Zolgensma Approval and Access June 2019 After Approval - Access 1. - - PowerPoint PPT Presentation

Zolgensma Approval and Access June 2019 After Approval - Access 1. Key Issues: A. Sites and capacity B. Insurance coverage C. Data 2. Broader Approval: A. Label vs Trials B. FDA did more than usual again (extrapolated for SMA) 3. Rules and


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Zolgensma Approval and Access June 2019

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SLIDE 2

After Approval - Access

  • 1. Key Issues:
  • A. Sites and capacity
  • B. Insurance coverage
  • C. Data
  • 2. Broader Approval:
  • A. Label vs Trials
  • B. FDA did more than usual again (extrapolated for SMA)
  • 3. Rules and Regulations:
  • A. Who can say what
  • B. US Only
  • C. Combinations and sequential (more at conferences)
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SLIDE 3

Public Treatment Sites

AL

  • Children’s of Alabama

AR

  • Arkansas Children’s Hospital

CA

  • Rady Children’s Hospital
  • UCLA

CT

  • Yale Pediatric Neuromuscular Clinic

FL

  • Nemours Childrens Hospital

IA

  • University of Iowa Stead Childrnens Hospital

IL

  • Ann and Robert Luri Children’s Hospital of Chicago

MA

  • Boston Children’s Hospital

MD

  • Johns Hopkins Hospital

MN

  • University of MN

MO

  • Washington University/St. Louis Children’s Hospital
  • Children’s Mercy Hospital

NC

  • Duke University Medical Center

NY

  • University of Rochester
  • SUNY Downstate Medical Center

OH

  • Nationwide Children’s Hospital
  • Cincinnati Children’s Hospital
  • Rainbow Babies and Children’s Hospital/University Hospitals of Cleveland

OR

  • OHSU Doernbecher Children’s Hospital

PA

  • Children’s Hospital of Philadelphia, Buerger Center for Advanced Pediatric Care
  • Clinic for Special Children

TX

  • University of Texas Southwestern/Children’s Health
  • Texas Children’s Hospital

UT

  • University of Utah/Primary Children’s Hospital

VA

  • Children’s Hospital of the King’s Daughters.

http://www.curesma.org/zolgensma-administration-sites.html treatments@curesma.org

27 sites consented 19 states

  • Updated daily

Goal is 50 to 100 sites

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SLIDE 4

FDA-Approved Label: INDICATIONS AND USAGE

ZOLGENSMA:

  • IV delivery AAV9 vector-based gene therapy

Approved for:

  • patients <2 years of age at dosing with

SMA verified by gene mutations or deletion in both survival motor neuron 1 (SMN1) genes

  • All types and all SMN2 copy numbers
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FDA-Approved Label: INDICATIONS AND USAGE

Limitations of ZOLGENSMA use:

  • 1. Repeat dosing of ZOLGENSMA has not been

evaluated

  • 2. The use of ZOLGENSMA in patients with advanced

SMA (e.g., complete paralysis of limbs, permanent ventilator dependence) has not been evaluated

  • 3. ZOLGENSMA should not be used in premature

infants due to neurologic developmental concerns related to using corticosteroids in premature infants

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Trial vs Label vs Policy

  • FDA label includes:
  • < 2 years of age at dosing
  • All copy numbers of SMN2
  • All types
  • Insurance

Coverage Policies ?

  • IV Clinical trials included:
  • < 9 months of age at dosing
  • Two copies of SMN2
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SLIDE 9

Insurance Coverage Publicly Available Policies

Payer Type 0 Type I Type II Type III Type IV 1 SMN2 2 SMN2 3 SMN2 4 SMN2 Coverage up to 2 years Coverage for advanced SMA Covers if prior Spinraza treatment Percentage of Coverage Commercial 0% Aetna 0% Anthem 0% Cigna 0% HCSC (BCBS) 0% BCBS MI 0% Humana 0% Molina 0% UnitedHealth No Yes No No No Yes Yes Yes No No No yes 38% Wellcare 0% Medicaid 0% AL 0% AK 0% AZ 0% AR 0% CA 0% CO 0% CT 0% DE 0% FL 0% GA 0% HI 0% ID 0% IL 0% IN 0% IA 0% KS 0% KY 0% LA 0% ME 0% MD 0% MA 0% MI 0% MN 0% MS 0% MO 0%

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SLIDE 10

Future Steps for Gene Therapy

1. Intrathecal (IT) delivery for older and bigger patients:

A. Differences to IV B. Current Clinical Trial: Study of Intrathecal Administration of AVXS-101 for Spinal Muscular Atrophy:

1) Clinicaltrials.gov Identifier: NCT03381729

2) Also known as STRONG 3) Phase1: 27 subjects at 11 sites in the US 4) 6 months to 60 months of age and three copies of SMN2 and symptoms < 12 months of age 5) Sit independently and not standing or walking independently 6) Three different dose cohorts

a. Currently enrolling for highest dose cohort C

7) Timing and FDA.

C. Potentially additional trials D. Data for FDA and Community and Coverage E. Potential timing and scope

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Timing and Waiting

1. Evaluate and discuss the following with your neurologist:

A. All available safety and efficacy data B. Method of administration C. Practical and process timing issues

2. Cure SMA recommends not waiting for a future treatment or trial option if other options are available now:

A. Earliest possible administration of SMN enhancing drugs yields best results B. Timing is one of the biggest factors in degree of response to SMN upregulation

3. Additional testing prior to dosing and insurance process will also factor into timing

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SLIDE 12

FDA-Approved Label: INDICATIONS AND USAGE

ACUTE SERIOUS LIVER INJURY Acute serious liver injury and elevated aminotransferases can

  • ccur with ZOLGENSMA.
  • Every child considered for ZOLGENSMA must have the

following blood tests prior to treatment:

  • AAV antibodies
  • Liver function tests
  • Platelet count
  • Troponin-I
  • ZOLGENSMA may be delayed or may not be given if any
  • f these results are abnormal.
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SLIDE 13

SMA and Care and Monitoring

  • Continue close follow up by an experienced

healthcare provider:

  • Monitor for symptoms of SMA
  • Monitor for side effects of treatments
  • Optimize the benefits of treatment
  • Discuss new information about SMA
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FDA-Approved Label: INDICATIONS AND USAGE

  • After treatment, blood tests are repeated as follows:
  • Liver function tests – weekly x 1 month, then every 2

weeks x 2 months until results normalize

  • Platelet count – weekly x 1 month, then every 2

weeks x 2 months

  • Troponin-I - weekly x 1 month, then monthly x 2

months

  • At 30 days, if liver function tests are abnormal the

prednisolone course is extended. See package

  • insert. Prednisolone dose must be tapered.
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SLIDE 15

Options and Choices

  • 1. A or B (A not B)
  • 2. A then B (B then A)
  • 3. A and B

Considerations:

  • Data whether benefits and what risks:
  • Trials, Anecdotes, Real World Evidence
  • Important to
  • Community, and
  • Coverage
  • More complicated when a treatment is permanent
  • Combination risks
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SLIDE 16

Resources

  • General Information:

– www.cureSMA.org/Zolgensma

  • Administration Site List:

– www.cureSMA.org/ZolgensmaSites

  • Choice and Connection to Care (insurance information*):

– http://www.curesma.org/support-care/care- publications/

  • Questions on Zolgensma or other treatment-related

inquiries:

– Email treatments@curesma.org

*Choice and Connection to Care provides general information on choosing and navigating insurance coverage.

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