Scientific Programme

Scientific
Programme


Short Oral Presentations

November 6, 2025 – Thursday
Eğitim – Klinik Araştırmalarda Risk Değerlendirmesi ve Biyobenzer Ürünlerde İmmünojenisite Testleri
Moderatorler: Uzm. Dr. Muhammed Emin Çelik, Prof. Dr. Nurşen Başaran
13.00-13.30 Faz I klinik çalışmalarını desteklemek için kullanılan klinik öncesi verilerin risk değerlendirmesi
Prof. Dr. Yalçın Duydu
13.30-14.00 Klinik araştırmalarda risk değerlendirme raporunda dikkat edilecek hususlar
Dr. Ecz. Hilal İlbars
14.00-14.30 İlaç sektörü açısından klinik araştırmalarda risk değerlendirmesinde karşılaşılan sorunlar
Dr. Mahir Kurt (Roche Türkiye)
14.30-15.00 Soru – Cevap
15.00-15.30 Kahve arası
Biyobenzer Ürünlerde İmmünojenisite Testlerinin Önemi
15.30-16.00 Biyobenzer ürünlerde immünojenisite testleri
Prof. Dr. Bensu Karahalil
16.00-16.30 Biyobenzer ürünlerde ruhsatlandırma
Prof. Dr. Alper İskit
16.30-17.00 Biyobenzer ürünlerde klinik araştırmalardaki güncel durum
Dr. Kim. Müh. Ayla Özsar
17.00-17.30 Biyobenzer ürünlerde karşılaşılan sorunlar
Dr. Hasan Ersin Zeytin (Yerlikaya Biopharma İlaç Sanayi ve Tic. A.Ş.)
18.00-18.20 Welcome
Congress Chair: Nurşen Başaran
President of TST: Yalçın Duydu
18.20-18.50 Opening Lecture
Chair: Ali Esat Karakaya
One health in the perspective of a toxicologist
Félix Carvalho (Portugal)
19.00-21.00 Opening Reception
November 7, 2025 – Friday
09.00-09.30 Plenary Lecture
Chair: Yalçın Duydu
Toxicological consideration and risk assessment of drug impurities
Biljana Antoijevic (Serbia)
SESSION 1: Transporters in Toxicology – Unraveling Mechanisms of Xenobiotic Exposure, Metabolic Dysfunction, and Reproductive Health
Chairs: José E. Manautou, Bensu Karahalil
09.30-10.00 Fetoplacental toxicity and mycoestrogens at the placental barrier
Lauren M. Aleksunes (USA)
10.00-10.30 Multidrug resistance protein 4 dysfunction drives hepatic steatosis and metabolic dysregulation: Integrated in vivo and in vitro insights
José E. Manautou (USA)
10.30-11.00 Integrating drug development tools to predict per- and polyfluoroalkyl (PFAS)-transporter interactions and disposition to human liver
Angela L. Slitt (USA)
11.00-11.15 Coffee break
SESSION 2: Epigenetic Mechanisms in Toxicology
Chairs: Sibel Özden, Benay Can Eke
11.15-11.45 Epigenetic biomarkers for chemical hazard assessment
Joëlle Rüegg (Sweden)
11.45-12.15 AHR-mediated m6A RNA methylation contributes to PM2.5-induced cardiac defects
Tao Chen (China)
12.15-12.45 Role of epigenetic modifications in the toxicity mechanisms of Fusarium-induced mycotoxins
Ecem Fatma Karaman (Türkiye)
12.45-14.00 Lunch Break
Industry Sponsored Workshop*
MatTek (Workshop brochure)
14.00-16.00 In vitro 3D reconstructed human skin tissue models and their use in toxicology and pharmacology
SESSION 3: New Approaches to In Vitro Efficacy/Toxicity Assessment – Advantages and Limitations
Chairs: Félix Carvalho, Merve Güdül Bacanlı
14.00-14.30 New air-liquid interface (ALI) system approach for drug efficacy/toxicity testing
Merve Güdül Bacanlı (Türkiye)
14.30-15.00 Challenges in implementing new approaches methodologies in the risk assessment of nanomaterials
Ivana Vinković Vrček (Croatia)
15.00-15.30 Organoid models to test drug safety and efficacy
Esra Erdal (Türkiye)
15.30-16.00 Advancements of in vitro methods for inhalation toxicity towards next generation risk assessment
Tommaso Serchi (Luxembourg)
16.00-16.15 Coffee Break
SESSION 4: Safety in Psychotropic Medications Treatment
Chairs: Sinan Süzen, Christoph Hiemke
16.15-16.45 Monitoring the safety and tolerability of antipsychotic drug treatment
Christoph Hiemke (Germany)
16.45-17.15 Comprehensive overview on intoxications with psychotropic drugs
Fredrik C. Kugelberg (Sweden)
17.15-17.45 Pharmacokinetic genes variations and response to treatment: the examples of risperidone, aripiprazole and clozapine
Eap-Bin Chin (Switzerland)
17.45-18.15 The impact of pharmacodynamic gene variations on adverse drug reactions in antidepressant treatment
Sinan Süzen (Türkiye)
SESSION 5: Advances in Food Safety and Risk Assessment: Emerging Challenges and Solutions
Chairs: Gülten Omurtag, Biljana Antoijevic
18.15-18.45 Toxic metals in food and their emerging role as risk factors in hormone-related reproductive cancers
Aleksandra Buha (Serbia)
18.45-19.15 Food safety risk assessment in Türkiye
Serap Hancı (Türkiye)
19.15-19.45 Challenges of the risk assessment of dietary microplastics
María-Carmen Rubio-Armendáriz (Canary Islands, Spain)
20.00 Dinner
November 8, 2025 – Saturday
09.00-09.30 Plenary Lecture
Chair: Onur Erdem
Toxicology risk management through interdisciplinary approaches to meet ESG requirements and sustainability challenges
Salmaan Hussain B Inayat Hussain (Malaysia)
09.30-09.45 Coffee Break
SESSION 6: The Importance of Genotoxicity Tests in the Biomonitoring of Chemical Hazards in Occupational Settings
Chairs: Mirta Milic, Aylin Üstündağ
09.45-10.10 The comet assay in human biomonitoring
Andrew Collins (Norway)
10.10-10.35 Alkaline comet and micronucleus cytome assay – Methods and Perspectives through HCOMET, HUMNAP, EDIAQI, AND BIOMOLTOX Projects
Mirta Milic (Croatia)
10.35-11.00 Steel industry in Bosnia and Herzegovina – Human biomonitoring in exposed population
Anja Haveric (Bosnia and Herzegovina)
11.00-11.25 Genotoxicity biomarkers in occupational exposure to hazardous compounds in Portugal: Lessons on formaldehyde, antineoplastics and volatile organic compounds
Carina Ladeira (Portugal)
11.25-11.50 Occupational exposure to mineral fibers – biomarkers of exposure, effect and susceptibility
Maria Dusinska (Slovakia/Norway)
12.00-13.30 Lunch break
SESSION 7: Cutting-edge Advances in NAMs – What’s New and What’s Next
Chairs: Emanuela Corsini, Özlem Atlı Eklioğlu
13.30-14.00 Advancing immunotoxicology: NAMs for immunosuppression and developmental immunotoxicity
Emanuela Corsini (Italy)
14.00-14.30 Advancing ocular safety: insights into the new OECD guideline
Helena Kandarova (Slovakia)
14.30-14.45 NAMs in cosmetics: the future of safety and innovation
Zehra Sarıgöl Kılıç (USA)
14.45-15.00 Computational and predictive analysis in toxicology
Sanin Haveric (Bosnia and Herzegovina)
15.00-15.15 Coffee Break
Introducing CAS (A division of the American Chemical Society) – Parallel Session
14.00-14.30 From Data to Discovery: Exploring the Role of CAS Solutions in Advancing Toxicological Research
Miriam Plana (from Spain)
SESSION 8: Microplastics – State of the Science and the Impacts on Human Health
Chairs: Neslihan Aygün Kocabaş, Erik Rushton
15.15-15.45 Understanding microplastics and human health concerns
Neslihan Aygun Kocabaş (Belgium)
15.45-16.15 Challenges of microplastics research in risk assessment: Ensuring generation of quality data
Erik Rushton (Netherlands)
16.15-16.45 Plastic chemical additives: determining human risk from microplastic exposure
John Norman (USA)
16.45-17.15 Microplastics: unfolding consequences
Marijana Curcic (Serbia)
SESSION 9: Advancements in Understanding the Mechanisms of Organ-Specific Toxicity Induced by Chemicals and Drugs
Chairs: Hilmi Orhan, Sinem Ilgın
17.15-17.45 New insight into molecular targets and early key events in genotoxicity and renal carcinogenicity of the mycotoxin ochratoxin A
Johannes Borchers (Germany)
17.45-18.15 Towards understanding the mechanism of methanol-induced optic nerve damage by leveraging human data
Hilmi Orhan (Türkiye)
18.15-18.45 Particle-induced acute phase response as a mechanism-of-action of particle-induced cardiovascular disease
Ulla Vogel (Denmark)
18.45-19.15 Human in vitro models for the detection and understanding of chemical-induced nephrotoxicity
Paul Jennings (The Netherlands)
20.00 Gala dinner
November 9, 2025 – Sunday
09.00-09.30 Plenary Lecture
Chair: Ahmet Aydın
Mode of action-based refined risk assessment for direct and indirect genotoxic carcinogens
Andrea Hartwig (Germany)
SESSION 10: European and National Regulation on Medical Devices – Challenges and Opportunities for Toxicologists
Chairs: Gül Özhan, Suna Sabuncuoğlu
09.30-10.00 Medical devices made of substances: challenges on definitions for classification and biosafety assessment
Marco Racchi (Italy)
10.00-10.30 Toxicological challenges for industry in the application of MDR 745/2017
Nina Eriksen (Denmark)
10.30-11.00 Methodological aspects for biosafety compliance in medical devices
Emanuela Testai (Italy)
11.00-11.30 Toxicological risk assessment for extractables/leachables in pharmaceuticals and medical devices
Ahmet Aydın (Türkiye)
Closing Ceremony
11.30-12.00 Closing ceremony

12th International Congress of the Turkish Society of Toxicology


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Secretariat

Prof. Dr. Özlem ATLI EKLİOĞLU
Anadolu University, Faculty of Pharmacy
Department of Toxicology
26210 Tepebaşı/Eskişehir/Turkey
ttdcongress@gmail.com
+90 (222) 335 0580 / 3755

Tunga Tour, 2021