Drug-Related Side Effects and Adverse Reactions clinical trials
The registry lists 449 studies for Drug-Related Side Effects and Adverse Reactions across more than 10 countries. 77 are recruiting or about to start. 241 of them are mainly about Drug-Related Side Effects and Adverse Reactions (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-10. Counting its 10 narrower conditions too, such as Cardiotoxicity: 1,116 studies, 249 open.
Get an email when these change. Save the Drug-Related Side Effects and Adverse Reactions studies recruiting or about to start — once a week, free: studies that open, close, add sites or post results.
See an example email
Example · made-up studies
Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
One email a week for all your saved searches. Stop any time.
Status
Who runs them
Brigham and Women's Hospital (7) · University of British Columbia (7) · Cipherome, Inc. (5) · VA Office of Research and Development (5) · Assistance Publique - Hôpitaux de Paris (5) · Hospices Civils de Lyon (4) · Samsung Medical Center (4) · Groupe Hospitalier Pitie-Salpetriere (4)
Who develops what
Save this setEvery programme with a company-led study here in the last two years, whatever its size: 3 programmes from 3 companies, 1 with this as their studies’ main aim; 0 with a live phase 3 study; 1 primary completion in the next 12 months.
Comparator & background therapies
What other companies’ phase 2+ studies give as the comparator or the background here (its leading trial sponsor and partners left out): a sign of what new drugs are measured against, not by itself the standard of care, its prescriptions or its market.
None given by two companies or more yet.
Programmes
“Meets, by arms” reads each study’s arms: vs its arm against the therapy’s; + X vs a combination against it; added to it plus the therapy against the therapy; studied with given together only. The next primary completion is the next phase-3 study’s when there is one.
The 3 programmes — sign in to see the whole list, free: filter by phase and aim, sort by late development, direct comparisons or the next primary completion.
Primary completion in the next 12 months (1)
Live phase 2 and 3 studies of these programmes. Primary completion is when the main measure’s data collection ends, as the registry states it (most are estimates); results come later, if they are announced.
- Dec 2026 est.GIPR Agonist LY3537021 · Eli Lilly and Company · Phase 2 named, not the main aimNCT07169851 A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With Cancer — primary endpoint: Proportion of Participants with a Complete Response (CR) in the Delayed Phase of CINV · 204 enrolled
Read from ClinicalTrials.gov, industry-led studies. Main aim: this is the study’s judged main condition; named, not the main aim: the sponsor names it, the study is about something else; registry mapping only: only the registry’s mapping put it here. Leading trial sponsor is the company leading the most industry studies of a drug, a measure of trial activity, not of rights. US and EU rights, and Approved: from the regulators’ records (FDA’s Drugs@FDA via openFDA; EMA’s medicines data) — the holder of a marketed or authorised original, generics and other companies’ versions; not rights elsewhere, nor approval for this condition. Phase 4 trial recorded, where neither lists it: a phase 4 study exists somewhere. Not read yet: labels by indication, exclusivity, licences, line of therapy, academic comparators, sales.
What is being tested here
Drugs under test in Drug-Related Side Effects and Adverse Reactions studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Nimotuzumab | 1 | 0 | 2 |
| Propofol | 1 | 1 | 2 |
| Ivermectin | 1 | 0 | 1 |
| Fexuprazan | 1 | 0 | 1 |
| Duloxetine | 1 | 1 | 1 |
| Furosemide | 1 | 1 | 1 |
| Vonoprazan | 1 | 0 | 1 |
| GIPR Agonist LY3537021 | 1 | 0 | 1 |
| Remimazolam besilate | 1 | 0 | 1 |
| Remimazolam | 1 | 0 | 1 |
Drug classes tested here Immune checkpoint inhibitors 2 open · Antimitotic agents 10 · Tyrosine kinase inhibitors (TKIs) 7 · Antimetabolites 7 · Alkylating agents 6
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.
The 10 nearest, phase 3 first
- Jan 2027Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial) · Phase 3 · University of Texas Southwestern Medical Center
- Jun 2027Melatonin for Prevention of Kidney Injury · Phase 3 · Rutgers, The State University of New Jersey
- Nov 2026The Texas Interprofessional Pharmacogenomics (IPGx) · Texas A&M University
- Dec 2026A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With Cancer · Eli Lilly and Company
- Dec 2026Effectiveness of a Pragmatic, Metabolic Care Clinic for Patients With Severe Mental Illness - The Meta Care Clinic · Bjorn H. Ebdrup
- Dec 2026NORTH-REG Dwell-Time Study · Jørgen Bjerggaard Jensen
- Dec 2026A Phase I Trial of Tumor-Associated Lymph Node T-Cell Injection With Advanced Malignant Solid Tumors · Guangzhou FineImmune Biotechnology Co., LTD.
- Dec 2026The Critical Care Recovery Program: Use of a Structured Clinic Visit to Reduce Adverse Drug Events in ICU Survivors · University of British Columbia
- Dec 2026Impact of Genetic Variants on the Toxicity of Antibody-Drug Conjugates in Locally Advanced or Metastatic Breast Cancer: The Role of the UGT1A1 Gene as a Predictive Biomarker of Therapeutic Response · Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental
- Dec 2026IMMUNO-FIT Observational Study · University Hospital Southampton NHS Foundation Trust
Who these studies take
Of the 55 Drug-Related Side Effects and Adverse Reactions studies recruiting now, 37 (67%) set no upper age limit and 15 (27%) stop at 75 or younger. 14 (25%) take children under 18. 1 (2%) are for women only and 0 (0%) for men only; 4 (7%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 12 (22%) | 12 (22%) |
| 18 | 48 (87%) | 47 (85%) |
| 30 | 44 (80%) | 43 (78%) |
| 40 | 44 (80%) | 43 (78%) |
| 50 | 44 (80%) | 43 (78%) |
| 65 | 47 (85%) | 46 (84%) |
| 75 | 46 (84%) | 45 (82%) |
| 85 | 40 (73%) | 39 (71%) |
Across all 449 studies, recruiting or not: 24% stop at 75 or younger and 16% at 65; 25% take children; 5% are for women only and 2% for men only; 16% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Drug-Related Side Effects and Adverse Reactions studies take
Of 18 phase 4 interventional studies under Drug-Related Side Effects and Adverse Reactions, half reached primary completion within 19 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Phase 4 | 19 mo17–37 · 18 studies | — | — |
| Interventional, no phase | 26 mo12–43 · 73 studies | — | 29 mo12–43 · 71 studies |
| Observational | 45 mo24–97 · 69 studies | — | 59 mo24–… · 65 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 16, 2026.
Results posted1
- Multi-hospital Electronic Decision Support for Drug-associated Acute Kidney InjuryNov 10, 2026NCT06264752
Newly registered2
- Safety of Vonoprazan-Amoxicillin Dual Therapy Versus Concomitant Quadruple Therapy for H. Pylori EradicationNov 9, 2026NCT07924098
- Efficacy and Safety of Oral Ivermectin for Genital WartsNov 3, 2026NCT07913321
Studies
Recruiting first, then most recently updated. Showing 50 of 449. Browse all 449 → or search them.
- Safety of Vonoprazan-Amoxicillin Dual Therapy Versus Concomitant Quadruple Therapy for H. Pylori EradicationRecruitingNCT07924098Phase 41 country
- A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With CancerRecruitingNCT07169851Phase 210 countries
- Efficacy and Safety of Oral Ivermectin for Genital WartsNot yet recruitingNCT07913321Not applicable1 country
- Real World Asparaginase Therapy ToxicityNot yet recruitingNCT070080271 country
- PRE-EMPTIVE PHARMACOGENOMICS IN ACUTE CARE SETTINGS WITH HEALTH ECONOMIC EVALUATIONS (PHOENIX TRIAL)RecruitingNCT06907784Not applicable1 country
- Compliance and Tolerance to Oral AntiBiotherapy in Osteoarticular Infections (OTABIO)RecruitingNCT052029641 country
- IPGx PILOT Whole Genome Sequencing Extension CohortRecruitingNCT067660711 country
- Reporting, Evaluating, Preventing and Treating the Cardiotoxicity Induced by Anticancer Drugs During a Specific Cardio-oncology Consult and Follow up in Routine CareRecruitingNCT038825801 country
- Multi-Agent Collaborative ADR Prediction With Human-Machine Decision ComparisonRecruitingNCT078088661 country
- Prospective Pharmacogenetic Cohort Study of CYP2D6 Metabolizer Phenotype, Analgesic Failure, and Adverse Effects in Postoperative Patients Receiving Tramadol by Elastomeric Infusion PumpRecruitingNCT078108161 country
- Gut Microbiota and Diarrhea in Breast Cancer Patients Receiving PyrotinibRecruitingNCT072649851 country
- GLP-1 Receptor Agonists and Early Proctologic Effects in Morbid ObesityNot yet recruitingNCT076687651 country
- Efficacy and Safety of Remimazolam Besylate for Sedation in Post-Non-Cardiac Surgery Patients Requiring Mechanical VentilationRecruitingNCT06575530Phase 41 country
- ADCX-020 for the Treatment of Patients With Locally Advanced or Metastatic CancersRecruitingNCT07238075Phase 12 countries
- Maximizing Quality of Life After Cancer Through RehabilitationNot yet recruitingNCT07622407Not applicable1 country
- Retrospective Kinetic Safety Evaluation of an Intravenous Micellar Excipient PlatformNot yet recruitingNCT076090691 country
- Nutritional + Usual Corticosteroids Randomized Trial for Immune-Related pneumoniA - Therapeutic Utilization EvaluationNot yet recruitingNCT07554885Not applicable1 country
- Impact of Genetic Variants on the Toxicity of Antibody-Drug Conjugates in Locally Advanced or Metastatic Breast Cancer: The Role of the UGT1A1 Gene as a Predictive Biomarker of Therapeutic ResponseRecruitingNCT075828871 country
- Linezolid Tolerance During the BPaL Regimen With Dosage Personalization Based on Therapeutic Drug Monitoring (TDM) During Multidrug-Resistant Tuberculosis TreatmentRecruitingNCT07477119Phase 41 country
- TDM for Optimized Outcome in Patients With mRCC.RecruitingNCT046593431 country
- Serious Gaming for Chemotherapy-induced Nausea and VomitingRecruitingNCT05838638Not applicable1 country
- National Active Surveillance Network and Pharmacogenomics of Adverse Drug Reactions in ChildrenRecruitingNCT004141151 country
- Integrating Pediatric Pharmacogenomic Testing Into the Canadian Health Care SystemRecruitingNCT042493751 country
- IMMUNO-FIT Observational StudyRecruitingNCT073549711 country
- AIManage Using an AI-driven CDS and ChatbotNot yet recruitingNCT07546357Not applicable1 country
- Telenursing for the Early Detection and Management of Side Effects Associated With Cyclin-Dependent Kinase Inhibitors in Breast Cancer PatientsRecruitingNCT07524829Not applicable1 country
- FENOX Trial (Comparative Effectiveness of Fexuprazan Co-therapy in Patients Receiving Non-Vitamin K Antagonist Oral Anticoagulants)Not yet recruitingNCT07497893Not applicable1 country
- Isoniazid-Related Hepatotoxicity in Clinical Practice: Incidence and PredictorsNot yet recruitingNCT074723481 country
- MEOP - Multidimensional Evaluations in Oncological PsychiatryNot yet recruitingNCT07406113
- Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)RecruitingNCT05358535Phase 31 country
- Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic LeukemiaRecruitingNCT055121691 country
- The Geriatric Emergency Department Pharmacologic Harm Prevention ProjectRecruitingNCT07216846Not applicable1 country
- Effectiveness of a Pragmatic, Metabolic Care Clinic for Patients With Severe Mental Illness - The Meta Care ClinicRecruitingNCT06624462Not applicable1 country
- A Real-World Study of Fecal Transplants for Cancer Therapy Side EffectsRecruitingNCT07319364Phase 11 country
- The Efficacy and Adverse Reactions of Neotetracycline in the Treatment of GNB InfectionsEnrolling by invitationNCT069901261 country
- Melatonin for Prevention of Kidney InjuryRecruitingNCT05084196Phase 31 country
- Clinical Determinants and Adverse Reactions to Tropicamide/Phenylephrine in Hospitalized Patients.RecruitingNCT071786001 country
- Interprofessional Pharmacogenomics (IPGx) Registry and RepositoryRecruitingNCT067265901 country
- The Texas Interprofessional Pharmacogenomics (IPGx)RecruitingNCT062197201 country
- Comparative Study of Tranexamic Acid Dosing in Cardiac SurgeryRecruitingNCT07164300Not applicable1 country
- Pharmacogenomics of Selective Serotonin Reuptake Inhibitor (SSRI)-Induced Behavioural ActivationRecruitingNCT067630811 country
- Pharmacogenomics-Supported Psychotropic Prescribing TrialRecruitingNCT06929533Not applicable1 country
- Evaluating Informatics-assisted Immune-related Adverse Event Detection to Improve Registration Onto a BiorepositoryRecruitingNCT06789601Phase 1/21 country
- Applying a Multidisciplinary Intervention for Drug Adequacy in an Intermediate Care Hospital (AMIDA-ICH)RecruitingNCT07015112Not applicable1 country
- Ofloxacin Concentration-toxicity Relationship in the ElderlyRecruitingNCT04496024Not applicable1 country
- Pharmacogenetic Testing of Patients With Unwanted Adverse Drug Reactions or Therapy FailureRecruitingNCT041545531 country
- A Phase I Trial of Tumor-Associated Lymph Node T-Cell Injection With Advanced Malignant Solid TumorsRecruitingNCT06716619Phase 11 country
- Cardiovascular Prevention Strategies in Elderly Patients With Cancer (CARTIER Clinical Trial)RecruitingNCT03711110Not applicable1 country
- Safe Stop Ipilimumab-nivolumab (IPI-NIVO) TrialRecruitingNCT05652673Not applicable1 country
- Safety & Efficacy of Baclofen for Alcohol Withdrawal in Chronic Liver Disease With Active Alcohol ConsumptionEnrolling by invitationNCT068406521 country