Sudden Infant Death clinical trials
The registry lists 80 studies for Sudden Infant Death across more than 10 countries. 14 are recruiting or about to start. 37 of them are mainly about Sudden Infant Death (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-09.
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Breast cancer · Recruiting: 2 came in, 3 changed
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A study of drug A after surgery for early breast cancer
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· Enrollment: 300 → 450 participants
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Who runs them
Shire (7) · REGENXBIO Inc. (6) · Denali Therapeutics Inc. (4) · University of Virginia (3) · Takeda (2) · Nantes University Hospital (2) · Green Cross Corporation (2) · University of Edinburgh (2)
What is being tested here
Drugs under test in Sudden Infant Death studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 5, phase 3 first
- Jun 2027An Extension Study of the Long-Term Safety, Tolerability, and Efficacy of Tividenofusp Alfa (DNL310) in Participants With Mucopolysaccharidosis Type II (MPS II) From Study DNLI-E-0002 or Study DNLI-E-0007 · Phase 3 · Denali Therapeutics Inc.
- Nov 2026Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT · Paul Szabolcs
- Jun 2027Get Social Media and Risk-Reduction Training · University of Virginia
- Aug 2027Infant Safe Sleep in Pediatric Emergency Depratment · State University of New York at Buffalo
- Sep 2027A Study of Secondary Immunodeficiencies in Adults With Blood Cancers in Kazakhstan Who Have a Weakened Immune System (K-SIDE Study) · Takeda
Who these studies take
Of the 9 Sudden Infant Death studies recruiting now, 4 (44%) set no upper age limit and 5 (56%) stop at 75 or younger. 7 (78%) take children under 18. 3 (33%) are for women only and 0 (0%) for men only; 2 (22%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 6 (67%) | 5 (56%) |
| 18 | 8 (89%) | 5 (56%) |
| 30 | 8 (89%) | 5 (56%) |
| 40 | 8 (89%) | 5 (56%) |
| 50 | 8 (89%) | 5 (56%) |
| 65 | 5 (56%) | 3 (33%) |
| 75 | 5 (56%) | 3 (33%) |
| 85 | 4 (44%) | 2 (22%) |
Across all 80 studies, recruiting or not: 63% stop at 75 or younger and 60% at 65; 79% take children; 16% are for women only and 28% for men only; 34% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Sudden Infant Death studies take
Of 15 interventional studies with no phase under Sudden Infant Death, half reached primary completion within 19 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Interventional, no phase | 19 mo10–45 · 15 studies | — | — |
Each figure is the month by which half the studies had reached primary completion, with the range in which the middle half did. Studies still running count until their last registry update; studies that stopped early are left out. Phase 1 includes early phase 1; observational means prospective or not stated, as retrospective and cross-sectional studies date a window of data rather than a study. How these figures are worked out
What changed recently
From the registry's own updates since Oct 13, 2026.
Started recruiting1
- Infant Safe Sleep in Pediatric Emergency DepratmentNov 4, 2026NCT07779512
Studies
Recruiting first, then most recently updated. Showing 50 of 80. Browse all 80 → or search them.
- An Extension Study of the Long-Term Safety, Tolerability, and Efficacy of Tividenofusp Alfa (DNL310) in Participants With Mucopolysaccharidosis Type II (MPS II) From Study DNLI-E-0002 or Study DNLI-E-0007Enrolling by invitationNCT06075537Phase 2/314 countries
- Infant Safe Sleep in Pediatric Emergency DepratmentRecruitingNCT07779512Not applicable1 country
- A Study of Secondary Immunodeficiencies in Adults With Blood Cancers in Kazakhstan Who Have a Weakened Immune System (K-SIDE Study)Not yet recruitingNCT078681071 country
- Supply Induced Demand in Intensive Care Unit: a Retrospective TrialNot yet recruitingNCT077684101 country
- Improving Pediatrician Counseling About Infant Safe Sleep Using the Electronic Medical RecordRecruitingNCT05503771Not applicable1 country
- Identification of Genetic Variants Associated With Unexpected Infant Death SyndromeRecruitingNCT062444331 country
- Social Media and Risk-reduction Training for Preterm Infant Care PracticesNot yet recruitingNCT07420686Not applicable1 country
- PEARL (PrEnAtal Enzyme Replacement Therapy for Lysosomal Storage Disorders)RecruitingNCT04532047Phase 11 country
- Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal DemiseRecruitingNCT037759541 country
- Longitudinal Study of Neurodegenerative DisordersRecruitingNCT033332001 country
- Data Collection Study of Patients With Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT With RICRecruitingNCT045283551 country
- Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCTRecruitingNCT01962415Phase 21 country
- The Impact of the Nurse-Led "My Baby is Safe" Educational ProgramNot yet recruitingNCT07037914Not applicable1 country
- Get Social Media and Risk-Reduction TrainingRecruitingNCT06618586Not applicable1 country
- Training About Sudden Infant Death SyndromeCompletedNCT06922682Not applicable1 country
- A Multi-cohort Study of Safety, Efficacy, PK and PD of GNR-055 in Patients With Mucopolysaccharidosis Type IIActive, not recruitingNCT05208281Phase 2/31 country
- Incorporation of Safe Sleep Education Into m-Health TechnologyCompletedNCT06074211Not applicable1 country
- A Study to Determine the Efficacy and Safety of Tividenofusp Alfa (DNL310) vs Idursulfase in Pediatric and Young Adult Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II)Active, not recruitingNCT05371613Phase 2/314 countries
- Social Media and Risk Reduction Teaching-Enhanced ReachCompletedNCT04387552Not applicable1 country
- Long-term Follow-Up for RGX-121Active, not recruitingNCT045973852 countries
- Apparent Life Threatening Events, Sudden Infant Death Syndrome and Muscarinic ReceptorsTerminatedNCT03278977Not applicable1 country
- RGX-121-3102 Gene Therapy in Participants With MPS II (Hunter Syndrome)Active, not recruitingNCT07236606Phase 31 country
- JessieHug Feasibility and Usability AssessmentTerminatedNCT06466148Not applicable1 country
- An Extension Study to Assess the Long-term Safety and Efficacy of Hunterase (Idursulfase Beta)CompletedNCT07344376Phase 31 country
- A Study of Tividenofusp Alfa (DNL310) in Pediatric Participants With Hunter SyndromeActive, not recruitingNCT04251026Phase 1/24 countries
- An Extension Study of HGT-HIT-045 Evaluating Long-Term Safety and Clinical Outcomes of Idursulfase-IT in Conjunction With Elaprase in Pediatric Participants With Hunter Syndrome and Cognitive ImpairmentCompletedNCT01506141Phase 1/23 countries
- The Effect of the Use of Mobile AppCompletedNCT07032402Not applicable1 country
- CAMPSIITE™ RGX-121 Gene Therapy in Subjects With MPS II (Hunter Syndrome)Active, not recruitingNCT03566043Phase 2/32 countries
- RGX-121 Gene Therapy in Children 5 Years of Age and Over With MPS II (Hunter Syndrome)CompletedNCT04571970Phase 1/22 countries
- Environmental Exposures and Sudden Unexpected Infant DeathActive, not recruitingNCT067087931 country
- MPS II ImmunophenotypingTerminatedNCT049762311 country
- A Study of Potential Treatment-Responsive Biomarkers and Clinical Outcomes in Hunter SyndromeCompletedNCT040075363 countries
- A Study of GC1111 in Hunter Syndrom PatientsCompletedNCT03920540Phase 31 country
- Effect of Crystalloids With Different SID on pH, and Urinary Electrolytes During General AnesthesiaCompletedNCT03507062Not applicable1 country
- Investigation of the Genetic Diseases in Infants With Unknown Cause of DeathActive, not recruitingNCT060602491 country
- Safety and Efficacy of HMI-203 in ERT-Treated Adults With MPS IIWithdrawnNCT05238324Phase 12 countries
- The Effect of Video-Assisted Sudden Infant Death Syndrome Prevention Training Program and Counseling Practice on Mothers' Knowledge Level and Self-efficacy: Randomized Controlled StudyStatus unknownNCT05823051Not applicable
- Phase I/II Pilot Study of Mixed Chimerism to Treat Inherited Metabolic DisordersTerminatedNCT01372228Phase 1/21 country
- Biomarkers for Hunter SyndromeTerminatedNCT013302771 country
- Ascending Dose Study of Genome Editing by the Zinc Finger Nuclease (ZFN) Therapeutic SB-913 in Subjects With MPS IITerminatedNCT03041324Phase 1/21 country
- Mucopolysaccharidosis Type II ObservationalWithdrawnNCT045918342 countries
- Infant Care Practices StudyCompletedNCT03494621Not applicable1 country
- Mucopolysaccharidosis Type II Natural HistoryCompletedNCT035297863 countries
- Comparing Children's Book to Brochures for Safe Sleep Education in a Home Visiting ProgramCompletedNCT02376673Not applicable1 country
- A Safety and Dose Ranging Study of Idursulfase (Intrathecal) Administration Via an Intrathecal Drug Delivery Device in Pediatric Patients With Hunter Syndrome Who Have Central Nervous System Involvement and Are Receiving Treatment With Elaprase®CompletedNCT00920647Phase 1/22 countries
- Study of Intrathecal Idursulfase-IT Administered in Conjunction With Elaprase® in Pediatric Patients With Hunter Syndrome and Early Cognitive ImpairmentCompletedNCT02055118Phase 2/37 countries
- Extension of Study TKT024 Evaluating Long-Term Safety and Clinical Outcomes in MPS II Patients Receiving IdursulfaseCompletedNCT00630747Phase 2/310 countries
- Iduronate-2-sulfatase Enzyme Replacement Therapy in Mucopolysaccharidosis II (MPS II)CompletedNCT00069641Phase 2/34 countries
- Safety and Clinical Outcomes in Hunter Syndrome Patients 5 Years of Age and Younger Receiving Idursulfase TherapyCompletedNCT00607386Phase 43 countries
- An Observational Study Evaluating Anti-Idursulfase Serum Antibody Response in Hunter Syndrome PatientsCompletedNCT008829213 countries