Scientific program

Scientific program

Thursday, 29 May 2025
10:30-17:00 Registration
17:00-17:30 Welcome coffee
17:30-20:30 Opening ceremony
Greeting of guests
„For HAE Patients” Award
Opening lecture
Chairs: Anna Erdei, Bruce Zuraw
I-01 Developing mRNA for therapy: My Journey
Katalin Karikó
20:30-22:00 Welcome reception
Friday, 30 May 2025
08:00-10:15 Scientific Session I.
Chairs: Alvin Schmaier, Tomaš Freiberger
08:00-08:30
I-02
The protease inhibitor Inter-α-trypsin inhibitor heavy chain 4 (ITIH4) as a compensatory inhibitor in plasma of hereditary angioedema patients
Steffen Thiel
08:30-08:45
O-01
Non-peptide bradykinin B2 receptor ligands possessing a quinolinyl moiety, or variants thereof: pharmacological properties and computational prediction of binding modes
François Marceau
08:45-09:00
O-02
Clinical validation of a novel biomarker assay to characterise bradykinin-mediated angioedema in prospective and biobank plasma samples
Evangelia Pardali
09:00-09:15
O-03
Impact of C1-inhibitor binding to endothelial cells on the regulation of vascular permeability
Sonia Caccia
09:15-09:30
O-04
Systemic inflammation biomarkers in different endotypes of angioedema
Johana Gil Serrano
09:30-09:45
O-05
Identification of candidate biomarkers for diagnosing and assessing the disease severity of type 2 hereditary angioedema via plasma N-glycomics
Yingyang Xu
09:45-10:00
O-06
Inhibition of Bradykinin Liberation by plasma Kallikrein inhibitors ameliorates vasogenic edema in experimental (Murine) cerebral malaria independent of and in addition to artesunate
Alvin Schmaier
10:00-10:15
O-07
Differentiating subtypes of angioedema with machine learning
Toan Do
10:15-10:45 Coffee break
10:45-13:00 Scientific Session II.
Chairs: Anastasios Germenis, Matija Rijavec
10:45-11:15
I-03
Incidental findings related to genes associated to HAE-nC1INH: How to proceed?
Anastasios Germenis
11:15-11:30
O-08
Clinical and genetic characterization of three families with homozygous SERPING1 mutations in hereditary angioedema
Asuman Çamyar
11:30-11:45
O-09
What can we learn from genome sequencing in HAE C1inh-nl?
Julie Gauthier
11:45-12:00
O-10
Preliminary demographic and clinical data from a cohort of Spanish HAE-C1INH patients: The GenomAEH Study
Mar Guilarte
12:00-12:15
O-11
Genetic double strike in C1INH deficiency Hereditary Angioedema: when rare become ultra rare - Patient case series from a monocentric Italian cohort
Paola Triggianese
12:15-12:30
O-12
Cosegregation study of kallikrein-kinin system genes in a cohort of 8 unrelated families with HAE-C1INH in Southern Spain
Krasimira Baynova
12:30-12:45
O-13
Identification of a novel XPNPEP2 variant associated with hereditary angioedema with normal C1-INH activity - A molecular insight
Sandra Nieto
12:45-14:15 Lunch break
14:15-15:45 Pediatric HAE Guideline
15:45-17:30 Poster Session I. P01-P29
with Coffee break

Chairs: Sladjana Andrejevic, Mauro Cancian, Danny Cohn, Timothy Craig
P-01Hereditary angioedema with normal C1Inh and PLG mutation treated with tranexamic acid : Beware of the risk of thrombosis
Bocquet Alexis
P-02Challenges of Diagnosis and treatment of recurrent angioedema from Nepal - The unseen struggle in resource-constrained settings
Dharmagat Bhattarai
P-03Why are some HAE patients more resistant to prophylaxis than others?
Shira Benor
P-04Hereditary angioedema due to factor XII mutation: clinical manifestations among males subjects
Delphine Gobert
P-05Acquired angioedema: A case of recurrent angioedema for two years after a successful treatment and normalization of the C1 inhibitor level
Sladjana Andrejevic
P-06The effect of surgical and interventional procedures on attack frequency in hereditary angioedema patients
Ecem Ay
P-07Investigating the risks of long-term glucocorticoid and attenuated androgen use in patients with angioedema: A systematic literature review
Thomas Buttgereit
P-08Unmet needs and systemic challenges of HAE pediatric patient families in Europe
Camelia Isaic
P-09Exploring the Impact of Psychological Burden in Hereditary Angioedema with the Pictorial Representation of Illness and Self Measure (PRISM) Tool
Delphine Gobert
P-10Lanadelumab leads to meaningful quality of life improvement and reduced productivity loss in patients with HAE: final results from the ENABLE Study
Emel Aygören-Pürsün
P-11Infection rates in patients with Hereditary Angioedema treated with garadacimab
Mauro Cancian
P-12NTLA-2002 mechanism of action, pharmacology, safety, and efficacy in hereditary angioedema
Danny M Cohn
P-13THERAPEUTIC TRENDS IN LONG-TERM PROPHYLAXIS IN ADULT HAE PATIENTS IN SERBIA 2020-2024
Radovan Mijanovic
P-14Garadacimab-mediated inhibition of activated factor XII does not increase risk of thrombosis in patients with HAE
Emel Aygören-Pürsün
P-15Rationale and design of the Garadacimab REAl-world Treatment outcomes of effectiveness, safety and quality-of-life in patients with hereditary angioedema (GREAT) study
Andrea Zanichelli
P-16Avoiding Misdiagnosis in Hereditary Angioedema: A Case Report
Irina Guryanova
P-17Acquired Angioedema Due to C1-Inhibitor Deficiency: Patient Experience and Assessment of Patient-Reported Outcome Measures
Andrea Zanichelli
P-18In Their Own Words, Patient Perspectives on Time to Feeling in Control of an HAE Attack
Douglas Jones
P-19Long-Term Prophylactic Treatment with Oral Deucrictibant Improves Disease Control and Health-Related Quality of Life in Participants with Hereditary Angioedema: CHAPTER-1 Open-Label Extension Study
Markus Magerl
P-20Sustained Therapeutic Exposure with Once-Daily Oral Deucrictibant XR Tablet for Prophylaxis of Hereditary Angioedema Attacks: Results of a Pharmacokinetics Study in Healthy Volunteers
Zhi-Yi Zhang
P-21Optical genome mapping for the identification of complex structural variants in hereditary angioedema due to C1-inhibitor deficiency
Roger Colobran
P-22Somatic variants and mosaicism in hereditary angioedema due to C1-inhibitor deficiency: implications for genetic counselling
Roger Colobran
P-23First Bulgarian Family with Hereditary Angioedema Due to Plasminogen Gene Mutation: Clinical Insights and Treatment Approaches
Alex Fam
P-24Bradykinin Dilemma: Angioedema or Mere Mimicry
Ferhat Maksudov
P-25Time to end of progression of hereditary angioedema attacks treated with sebetralstat
William R. Lumry
P-26Clinical investigation of hereditary angioedema linked to coagulation factor XII mutations in a southern Spanish cohort
Teresa De Aramburu Mera
P-27Genetic segregation study in patients with hereditary angioedema due to mutation in coagulation factor XII in a population of southern Spain.
Teresa De Aramburu Mera
P-28Quality of Life in elderly patients affected by Hereditary Angioedema: data from the ITACA Register
Francesca Perego
P-29Impact of injectable HAE on-demand treatments on health-related quality of life: a patient and caregiver interview study
Patrick Yong
Saturday, 31 May 2025
08:00-10:00 Scientific Session III.
Chairs: Teresa Caballero, William Lumry
08:00-08:15
O-14
Preliminary results from Epidemiological survey of hereditary angioedema in India- just a tip of the iceberg
Ankur Kumal Jindal
08:15-08:30
O-15
HAE with normal C1Inh (HAE-n C1INH) and spontaneous mast cell AE (AE-MC): Clinical similarities and differences
Alexis Bocquet
08:30-08:45
O-16
Complement characteristics in angioedema due to acquired C1-inhibitor deficiency: A clinico-biological correlation
Leo Guennoun
08:45-09:00
O-18
Hereditary angioedema: A national investigation of associated comorbidities and surgical procedures
Lili Voloncs-Mindszenthy
09:00-09:15
O-19
Clinical expressions, disease course, quality-of-life and resilience in subgroups of patients with angioedema
Iris Leibovich-Nassi
09:15-09:30
O-20
Triggers in focus: A deep dive into what sets off HAE attacks
Adil Bahadir
09:30-09:45
O-21
Angiotensin converting enzyme inhibitor angioedema in an African population, a case control cohort
Cascia Day
09:45-10:00
O-22
Psychometric study of specific questionnaires HAE-QoL and AE-QoL and the generic questionnaire EQ-5D-5L in adult patients with hereditary angioedema due to C1 inhibitor deficiency
Teresa Caballero
10:00-10:30 Coffee break
10:30-12:30 Scientific Session IV.
Chairs: Markus Magerl, Marc Riedl
10:30-11:00
I-04
Body vs. Antibody – Behavior of monoclonal therapeutic antibodies in Angioedemas
László Cervenak
11:00-11:15
O-23
Long-term efficacy and safety of prophylactic treatment with once-daily deucrictibant for angioedema due to acquired C1-inhibitor deficiency: final study results
Mats de Lange
11:15-11:30
O-24
Garadacimab-mediated inhibition of activated factor XII had no impact on haemostasis in patients with hereditary angioedema
Timothy J. Craig
11:30-11:45
O-25
Lanadelumab shows infrequent injection site reactions and high patient satisfaction in patients with HAE: ENABLE Study Results
Mauro Cancian
11:45-12:00
O-26
Reduction in percentage of days with angioedema symptoms among young children initiating berotralstat: Interim results from APeX-P
Tamar Kinaciyan
12:00-12:15
O-27
Lanadelumab’s enduring impact on HAE attack reduction and improved disease control: final results from the ENABLE Study
Andrea Zanichelli
12:15-12:30
O-28
Normalization of elevated D-dimer with donidalorsen treatment across phase 2 and phase 3 studies in patients with hereditary angioedema
Andrea Zanichelli
12:30-14:00 Lunch break
14:00-16:15 Scientific Session V.
Chairs: Anete S. Grumach, Connie Katelaris
14:00-14:30
I-05
Assessment of risk and benefit in clinical trials: Challenges in rare diseases
Bruce Zuraw
14:30-14:45
O-29
Effectiveness of sebetralstat for the on-demand treatment of mucosal hereditary angioedema attacks: interim analysis from KONFIDENT-S
Henriette Farkas
14:45-15:00
O-30
Navenibart for Hereditary Angioedema (HAE): analysis of safety, pharmacokinetic, and pharmacodynamic data from Phase 1a and Phase 1b/2 ALPHA-STAR trial
Marc A. Riedl
15:00-15:15
O-31
HAELO, a phase 3, global, randomised, double-blind, placebo-controlled study of NTLA-2002, a CRISPR-based gene editing therapy, in participants with hereditary angioedema
Emel Aygören-Pürsün
15:15-15:30
O-32
Anxiety associated with hereditary angioedema attacks: results from the phase 3 KONFIDENT trial of oral sebetralstat
Timothy J. Craig
15:30-15:45
O-33
Long-term safety and efficacy of oral deucrictibant for prophylaxis in hereditary angioedema: data snapshot results of the chapter-1 open-label extension study
Emel Aygören-Pürsün
15:45-16:00
O-34
Long-term safety and efficacy of oral deucrictibant for treatment of hereditary angioedema attacks: Results of the rapide-2 extension study
Marc A. Riedl
16:00-16:15
O-35
ADX-324, a Q6-month SC investigational siRNA targeting Prekallikrein for HAE attack prevention
Robert MacLeod
16:15-17:45 Poster Session II. P30-P58
with Coffee break

Chairs: Sandra Christiansen, Stefan Cimbollek, Milos Jesenak, Hilary Longhurst
P-30Epidemiology of Bradykinin-Mediated Angioedema in the European Population
Emel Aygören-Pürsün
P-31Assessing the diagnostic value of complement testing in Type I Hereditary Angioedema in a pediatric population
Monica Colque-Bayona
P-32Survey results from Italy, the US, UK, and France: Anxiety in patients using injectable on-demand treatments for hereditary angioedema attacks
Mauro Cancian
P-33Limited access to On-Demand Treatment for Hereditary Angioedema has an impact on Quality of life: a comparison between two income settings
Cascia Day
P-34Physician and Patient level of agreement in hereditary angioedema attack reporting among a real-world European population
Mauro Cancian
P-35Physician-reported outcomes versus location of attack in a real-world hereditary angioedema patient population in Europe
Laurence Bouillet
P-36Distinct SERPING1 Variants and Genetic Modifiers Influencing Disease Expression in Hereditary Angioedema due to C1-Inhibitor Deficiency
Matija Rijavec
P-37Bioequivalence of lanadelumab 300 mg subcutaneous injection administered via the pre-filled syringe and pre-filled pen
Irmgard Andresen
P-38Impact of sex on the course of hereditary angioedema due to C1 inhibitor deficiency
Hanga Réka Horváth
P-39Candidate variants associated with Hereditary Angioedema with normal C1-Inhibitor
Helena Jakopič
P-40Effect of COVID-19 Infection on Hereditary Angioedema (HAE) – Survey of Canadian Patients
Amarjot Kang
P-41Increased risk of systemic lupus erythematosus in individuals with hereditary angioedema: a family study
Linda Sundler Björkman
P-42CHAPTER-3 Phase 3 Trial Design: Efficacy and Safety of the Oral Bradykinin B2 Receptor Antagonist Deucrictibant Extended-Release Tablet for Prophylaxis of Hereditary Angioedema Attacks
Andrea Zanichelli
P-43Genetic features of bradykinin-forming cascade and vascular endothelium permeability regulation pathways in Brazilian families with recurrent angioedema
Clarissa A. Bittencourt
P-44Utility of Abdominal Ultrasound in the Diagnosis of Abdominal Angioedema
Fiorella Adrianzen
P-45Phenotype and SERPING1 genotype of a cohort of 46 unrelated families with HAE-C1INH from Southern Spain
Krasimira Baynova
P-46Genetic insights in pediatric Hereditary Angioedema: Two cases treated with lanadelumab
Laurel-Laurel Rolando
P-47An update on SERPING1 variants identified in Hungarian patients with hereditary angioedema, including patients with two alterations and novel variants
Ágnes Szilágyi
P-48Atypical Presentation of Hereditary Angioedema- A Case of HS3ST6 Mutation with Uncommon Symptoms and Normal C1-INH Levels
Sandra Nieto
P-49First comprehensive report of hereditary angioedema due to C1 inhibitor deficiency in Bosnia and Herzegovina: one novel mutation and genotype-phenotype association
Mensuda Hasanhodzic
P-50Hereditary Angioedema Breakthrough: FXII Mutation Discovery and the Power of Icatibant and Lanadelumab
Eyal Ben Dori
P-51Development of a WB-based method to quantify different forms of C1INH in HAE-C1INH-Type2, based on the example of the R444C variant
Bence Farkas
P-52Uncovering Urinary Protein Biomarkers for Early Diagnosis and Evaluation of Hereditary Angioedema
Yuxiang Zhi
P-53Proactive identification of rare diseases: Lessons from hereditary angioedema diagnosis using electronic medical records
Xue Wang
P-54Factors Influencing Quality of Life in Angioedema Due to C1-Inhibitor Deficiency: A Single-Center Experience
Riccardo Senter
P-55Safety and Efficacy of Oral Deucrictibant for Treatment of Upper Airway and Laryngeal Hereditary Angioedema Attacks: Results from the RAPIDe-2 Extension Study
Ramon Lleonart Bellfill
P-56Durability of response to a single dose of oral deucrictibant for on-demand treatment of hereditary angioedema attacks
Anna Valerieva
P-57DEFICIT-syndrome, a novel entity in cerebral vasogenic oedema
Simon Péter Nagy
P-58Hereditary Angioedema (HAE) and Post Traumatic Stress Disorder (PTSD)
Sandra Christiansen
Sunday, 1 June 2025
08:00-09:30 Scientific Session VI.
Chairs: Ankur Jindal, Laurence Bouillet
08:00-08:15
O-36
Transient hepatitis after discontinuation of danazol in patients with hereditary angioedema due to C1-inhibitor deficiency: a case series
Danny Cohn
08:15-08:30
O-37
Very long-term efficacy of oral Berotralstat-LTP in hereditary angioedema patients
Tamar Kinaciyan
08:30-08:45
O-38
Tolerability and effectiveness of Berotralstat for Prophylaxis in adolescents with hereditary angioedema: Subgroup analysis of the berolife study
Isabelle Boccon-Gibod
08:45-09:00
O-39
Long-term prophylaxis usage for hereditary angioedema by Canadian physicians
Natasha Correa
09:00-09:15
O-40
Berotralstat for the prevention of hereditary angioedema attacks: Results from the Italian expanded access programme
Riccardo Senter
09:15-09:30
O-41
Real-world effectiveness of lanadelumab in hereditary angioedema in Slovakia – a 4-year experience
Milos Jesenak
09:30-10:00 Coffee break
10:00-11:30 Scientific Session VII.
Chairs: Paul Keith, Tamar Kinaciyan
10:00-10:15
O-42
Harnessing innovation to collect data for Harpe, a dynamic French registry of patients with hereditary angioedema: results from the single-centre phase
Alexis Bocquet
10:15-10:30
O-43
Turkish National hereditary angioedema and acquired angioedema registry, HAE/AAE-TR
Nihal Mete Gökmen
10:30-10:40
O-44
Case report: A 5-year-old boy with a truncating ANGPT1 mutation, possibly associated with hereditary angioedema with normal C1 inhibitor
Christina Weber-Chrysochoou
10:40-10:50
O-45
Clinical evidence for a cross-talk between mast-cells and bradykinin-mediated angioedema: Case report and discussion
Avner Reshef
10:50-11:00
O-46
Ureteral edema and hydronephrosis associated with hereditary angioedema attack
Züleyha Galata
11:00-11:10
O-47
The reduction of hereditary angioedema attacks following significant weight loss achieved through bariatric surgery
Marko Barešić
11:10-11:20
O-48
Hereditary angioedema and autoimmune thyroiditis in a preadolescent female
Gabriel E. Arce-Estrada
11:20-11:30
O-49
Is angioedema a clinical manifestation of immunodeficiency? Angioedema in heterozygous mutation of the PIK3R1 gene
Vania María Miranda Saavedra
11:30-12:15 Closing Remarks
12:15-14:00 Lunch
14:00- Departure