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NCT06370715Befejeződött4. fázis

A Study of LY900014 in Adult Participants With Type 2 Diabetes Mellitus in India

A 26- Week, Multicenter, Open-Label, Single-Arm, Phase 4 Study to Assess The Safety of Lyumjev in Adult Patients With Type 2 Diabetes Mellitus in India

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. szept. 28.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

The purpose of this study is to assess the safety of insulin lispro-aabc in adult participants with Type 2 diabetes mellitus in India. The study will last about 33 weeks for each participant, including screening (1 week), Lead-in period (4 weeks), treatment period (26 weeks) and follow up period (2 weeks).

Állapot (regiszter)
Befejeződött
Fázis (regiszter)
4. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
153 (tényleges)
Első benyújtás
2024. ápr. 15.
Kezdés
2024. ápr. 18.
Elsődleges befejezés
2025. szept. 2.
Fő szponzor
Eli Lilly and Company
NCT-szám
NCT06370715

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 4. fázis
  • Bevont résztvevők: 153
  • 2024. ápr. 18. és az elsődleges befejezés (2025. szept. 2.) között
  • 12 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Have had any episode of severe hypoglycemia (defined as requiring assistance due to neurologically disabling hypoglycemia) within the 6 months prior to screening
  • Have had 1 or more episodes of diabetic ketoacidosis or hyperglycemic hyperosmolar state within the 6 months prior to screening
  • Excessive insulin resistance defined as having received a total daily dose of insulin >2.0 U/kg at the time of screening
  • Have cardiovascular disease, within the past 6 months prior to screening, defined as stroke, decompensated heart failure (New York Heart Association Class III or IV), myocardial infarction, unstable angina pectoris, or coronary arterial bypass graft
  • Currently receiving renal dialysis
  • Have had a blood transfusion or severe blood loss within 90 days prior to screening or have known hemoglobinopathy, anemia, or any other traits known to interfere with measurement of HbA1
  • Have used thiazolidinediones, glucagon-like peptide 1 receptor agonist, or pramlintide within 90 days prior to screening

Más betegség

  • Having any other condition (including known drug or alcohol abuse, psychiatric disorder including eating disorder) that precludes the subject from following and completing the protocol
  • Have been diagnosed, at any time, with type 1 diabetes mellitus (T1DM) or latent autoimmune diabetes in adults
  • Have a known diagnosis of secondary diabetes (for example, diabetes caused by hemochromatosis, acromegaly, chronic pancreatitis, or pancreatectomy)
  • Have a history of or are being evaluated for bariatric surgery including Roux-en-Y gastric bypass surgery, gastric banding, and/or gastric sleeve
  • History of renal transplantation
  • Have obvious clinical signs or symptoms of liver disease (for example, acute or chronic hepatitis or cirrhosis), or elevated liver enzyme measurements
  • Have active or untreated malignancy, have been in remission from clinically significant malignancy (other than basal cell or squamous cell skin cancer) for less than 5 years, or are at an increased risk for developing cancer or a recurrence of cancer in the opinion of the investigator

Laborértékek

  • Serum creatinine >2.0 mg/dL (177 µmol/L) at screening
  • Have presence of clinically significant gastrointestinal disease (for example, clinically active gastroparesis associated with wide glucose fluctuations) in the investigator's opinion

Egyéb

  • Have hypoglycemia unawareness as judged by the investigator

Kiket keres a vizsgálat

  • Have Type 2 Diabetes Mellitus (T2DM) for ≥1 year prior to screening
  • Treated for ≥90 days prior to screening with multiple daily injection (MDI) therapy
    • on basal insulin or insulin glargine 100 U/mL [Basaglar or Lantus] or insulin glargin 300 U/mL, insulin determir, insulin degludec U-100, or neutral protamine Hagedorn (NPH) insulin) in combination with at least 1 prandial injection of bolus insulin (insulin lispro 100 U/mL or 200 U/mL, insulin aspart, insulin glulisine, regular insulin, fast-acting insulin aspart), or
    • premixed analog or human insulin regimens with any basal and bolus insulin
  • May have been treated with up to 3 oral antihyperglycemic medications (OAMs) including metformin, sodium-glucose cotransporter (SGLT)-2 inhibitor in accordance with local regulations. The dose of all OAMs must have been stable for ≥90 days prior to screening
  • Have an HbA1c value ≥7.5% and ≤10% according to the central laboratory at screening
  • Body mass index ≤45.0 kg/m²
  • Have access to a telephone, or alternative means for close monitoring/communications
  • Have refrigeration at home or have ready access to refrigeration for storage of insulin therapy
  • Have a regular wake-sleep schedule (awake-work during the day and sleep during the night)

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (12)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Vijyaratna Dibetes Diagnosis Treatment CentreAhmedabadIndiaIsmeretlen állapot
Center for Diabetes and Endocrine CareBengaluruIndiaIsmeretlen állapot
S. P. Medical College & A G HospitalBikanerIndiaIsmeretlen állapot
Kovai Diabetes Speciality Center and HospitalCoimbatoreIndiaIsmeretlen állapot
Osmania Medical College & HospitalHyderabadIndiaIsmeretlen állapot
Rajasthan University of Health SciencesJaipurIndiaIsmeretlen állapot
Brij Medical Center Pvt. Ltd.KanpurIndiaIsmeretlen állapot
Medical College & Hospital, KolkataKolkataIndiaIsmeretlen állapot
Chellaram Diabetes InstitutePuneIndiaIsmeretlen állapot
Sahyadri Super Speciality HospitalPuneIndiaIsmeretlen állapot
Diabetes Research CentreRoyapuramIndiaIsmeretlen állapot
King George Hospital, VisakhapatnamVisakhapatnamIndiaIsmeretlen állapot

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