Genotype and dose-dependent response to ... - Mirum Pharma · PFIC is a group of genetic...
Transcript of Genotype and dose-dependent response to ... - Mirum Pharma · PFIC is a group of genetic...
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Genotype and dose-dependent response to maralixibat in patients with bile salt export pump
deficiency
Richard Thompson, Kings College London, London, UK
Thomas Jaecklin, Chris Peetz, Pamela Vig on behalf of the LUM001-501 INDIGO Study Group
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Author disclosures
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I disclose the following financial relationships with commercial interest:
Consultancy
Mirum, Albireo Pharma, GenerationBio, Qing Bile Therapeutics, Horizon Pharma, Alnylam, Sana Biotechnology
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Qing Bile Therapeutics, GenerationBio
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PFIC is a group of genetic progressive liver diseases
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• PFIC is associated with:
- debilitating pruritus, growth deficit, lipid-soluble vitamin deficiency, progressive liver disease
• If medical management fails:
- partial external biliary diversion surgery or liver transplant for pruritus
Aim
• To investigate the response to pharmacological interruption of the enterohepatic circulation of
bile acids in BSEP deficiency
Methods
• Analysis of treatment response from maralixibat Phase 2 INDIGO trial in children with PFIC due to
bile salt export pump (BSEP) deficiency
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Natural history background: NAPPED outcomes post PEBD
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1. Van Wessel, EASL/ILC 2019 https://easl.meta-dcr.com/ilc2019/slides?page=1&q=napped,;
sBA levels <100 μM post-biliary diversion predict transplant-free survival1
Transplant-free survival after biliary
diversion is associated with genotype
Early post-surgical sBA associated with
transplant-free survival
(Truncating)
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Maralixibat: an oral, minimally absorbed, selective inhibitor of
ASBT (apical sodium-dependent bile acid transporter)
Redirects bileacid flow by inhibiting
reuptake by ASBT
Interrupts recirculation of bile acids to the liver
Increases fecal bile acid excretion
Clinical effects seen
in cholestasis
ASBTi clinical studies show:
✓ Reductions in pruritus
✓ Reduction in sBA
✓ Impact on markers of bile
acid synthesis:
cholesterol, C4, FGF19
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Abbreviations: sBA: serum bile acid; ASBT: apical sodium-dependent bile acid transporter
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INDIGO: Open-label Phase 2 Study of Maralixibat in PFIC
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Week 13 & Week 48
analyses
INDIGO Phase 2•N = 33 children with PFIC
• 8 FIC1 def (PFIC1)
• 25 BSEP def (PFIC2)
• 10 sites in 4 countries
Maralixibat
280 µg/kg
Once daily
Long-term
extension
Dose increased
Maralixibat
280 µg/kg
Twice daily
Endpoints:• Serum bile acids, pruritus, QoL, growth
• Safety and tolerability
Analysis of long-term treatment response in the BSEP deficient group
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Patient disposition, demographics, disease characteristics
Patient characteristics BSEP Genetic Status
N=33PFIC1, n = 8
FIC1 def
PFIC2, n = 25
BSEP def
Median age
(range), year2.0 (1–7) 4.0 (1–13)
Boys, n (%) 6 (75) 8 (32)
White, n (%) 6 (75) 20 (80)
Serum bile acid
(range), µmol/L
261.9
(159.8-423.5)
381.0
(34.4-602.1)
Mean (SD) z-scores
Height –2.96 (1.47) –1.29 (0.98)
Weight –2.70 (2.82) –0.63 (0.88)
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Participants
(n)
Non-truncating
(mild/moderate)19
Truncating 6
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INDIGO: Multi-parameter response in BSEP deficiency
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Subject Genotype StatusMulti-parameter
Responders
Non-truncating BSEP (N=19) 7/19 (36.8%)
Mild (N=7) 1/7 (14.3%)
Moderate (N=12) 6/12 (50%)
Truncating BSEP (N=6) 0/6 (0%)
*ItchRO Observer Score: 0-4 observer-rated pruritus scale,
RESPONDER DEFINITION:
• ≥ 70% reduction or normalization of sBA
AND
• ≥1.0 reduction in ItchRO(Obs)*
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Serum bile acid responses differ by BSEP mutation status
The black filled circle refers to termination. The white filled circle refers to the start of BID dosing (280µg/kg BID)
Long-term extension
sBA responders maintain response long-term with maralixibat
Non-truncating (nt) BSEP mutations Truncating BSEP mutations
Long-term extension
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Non-truncating BSEP subjects: long-term pruritus response
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Long-term extension
The black filled circle refers to termination The white filled circle refers to the start of BID dosing (280µg/kg BID)ItchRO Observer Score: 0-4 observer-rated pruritus scale
KEY POINTS
• 12 patients into 5th year of treatment
• >50% (10/19) patients with ≥1.0 pt reduction
• ItchRO(Obs) response is sustained over years
Study Day
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Non-truncating BSEP responders showed significant increases in 7α-hydroxy-4-cholesten-3-one (C4)
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Mean C4 levels (ng/ml) –
log10 scale
The black filled circle refers to termination. The white filled circle refers to the start of BID dosing (280µg/kg BID)
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Non-truncating BSEP responders had significantly different C4 to serum bile acid ratios vs non-responders
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C4 to Serum
Bile Acid Ratio –
change from baseline,
log10 scale
The black filled circle refers to termination. The white filled circle refers to the start of BID dosing (280µg/kg BID)
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Non-truncating BSEP responders had significantly different C4 to serum bile acid ratios vs non-responders
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C4 to Serum
Bile Acid Ratio –
change from baseline,
log10 scale
The black filled circle refers to termination. The white filled circle refers to the start of BID dosing (280µg/kg BID)
C4/sBA response on dose elevation
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Non-truncating BSEP responders had significantly different C4 to serum bile acid ratios vs non-responders
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C4 to Serum
Bile Acid Ratio –
change from baseline,
log10 scale
The black filled circle refers to termination. The white filled circle refers to the start of BID dosing (280µg/kg BID)
Partial-C4/sBA response; potential benefit with increased dose
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Conclusions
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• Change in C4/serum bile acid ratio is good predictor of response to ASBTi
• Initial non-responders may benefit from increased doses of maralixibat
- Particularly those with greater BSEP function (i.e. mild mutation)
- Patients predicted to have biallelic truncating mutations show no response, in
line with results from partial external biliary diversion surgery
• Patients with non-truncating BSEP deficiency can have durable control of
pruritus and cholestasis with maralixibat
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We thank the members of the INDIGO / LUM001-501 study group
- Professor Irena Jankowska Children's Memorial Health Institute, Warsaw, Poland.
- Professor Deirdre Kelly Birmingham Children’s Hospital, Birmingham, UK
- Dr Kathleen Loomes Children’s Hospital of Philadelphia, University of Pennsylvania Medical School, PA, USA
- Dr Cara Mack Children’s Hospital Colorado, University of Colorado School of Medicine,
Aurora, CO, USA
- Dr Alexander Miethke Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of
Medicine, Cincinnati, OH, USA
- Dr Sanjay Rajwal Leeds Children’s Hospital, Leeds, UK
- Dr Christine Rivet Hôpital Femme Mère Enfant, Hospices Civils du Lyon, Bron, France
- Professor Kenneth Setchell Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of
Medicine, Cincinnati, OH, USA
- Dr Nisreen Soufi Children’s Hospital Los Angeles, University of Southern California, Los Angeles, CA, USA
- Professor Robert Squires Children’s Hospital of Pittsburgh, University of Pittsburgh School of Medicine, PA, USA
Acknowledgements
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Thank You!