foscarnet / Generic mfg. 
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10 Trials

   

Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
foscarnet / Generic mfg.
2007-003472-19: Determining a viral load threshold for pre-emptive therapy for cytomegalovirus infection in transplant patients using real time PCR monitoring.

Ongoing
4
178
Europe
foscarnet, Ganciclovir, valganciclovir, Intravenous infusion, Powder for injection*, Film-coated tablet, Foscavir, Cymeve IV, Valcyte 450mg film-coated tablets
Royal Free Hampstead NHS Trust
Transplant recipients with CMV infection.
 
 
NCT03004261: CMV-CTL for the Treatment of CMV Infection After HSCT

Completed
4
5
RoW
donor derived cytomegalovirus specific T lymphocytes, cytomegalovirus specific T lymphocytes, Foscarnet, Ganciclovir
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai iCELL Biotechnology Co., Ltd, Shanghai, China
Cytomegalovirus Infections, Hematological Disease
12/21
12/21
PRIOH-1, NCT03073967 / 2020-004940-27: Trial on Efficacy and Safety of Pritelivir Tablets for Treatment of Acyclovir-resistant Mucocutaneous HSV (Herpes Simplex Virus) Infections in Immunocompromised Subjects

Recruiting
3
153
Europe, Canada, US, RoW
Pritelivir, Investigator's choice, Foscarnet or Cidofovir or Imiquimod
AiCuris Anti-infective Cures AG, Medpace, Inc.
HSV Infection
01/25
04/25
NCT06439342: A Study of Maribavir in Chinese Adults With Cytomegalovirus (CMV) Infections

Not yet recruiting
3
20
RoW
Maribavir, TAK-620
Takeda
Cytomegalovirus (CMV)
02/27
02/27
ChiCTR-TRC-11001683: Perioperative hepatitis B virus load control strategies and molecular mechanisms of anti-recurrence and metastasis in hepatic cancer

Completed
2
200
 
Give lamivudine antiviral therapy ;Give lamivudine and foscarnet antiviral therapy ;Give lamivudine and adefovir dipivoxil antiviral therapy ;Give entecavir antiviral therapy
1st Affiliated Hospital of Medical College, Zhejiang University; Zhejiang University School of Medicine, self
hepatic cancer and hepatitis B virus
 
 
2011-001449-34: Study for the treatment of cytomegalovirus infection, in transplanted patients Estudio para el tratamiento de la infeccion por citomegalovirus, en pacientes trasplantados.

Ongoing
2
64
Europe
GANCICLOVIR, FOSCARNET, VALGANCICLOVIR, CYMEVENE, FOSCAVIR, VALCYTE, CYMEVENE, FOSCAVIR, VALCYTE
FUNDACION INVESTIGACION HOSPITAL CLINICO DE VALENCIA-INSTITUTO DE INVESTIGACION SANITARIA INCLIVA, Ministerio de Sanidad y Politica Social
Cytomegalovirus infection in patients treated with hematopoietic allogenic transplant INFECCION POR CITOMEGALOVIRUS EN PACIENTES TRATADOS CON TRASPLANTE HEMATOPOYETICO ALOGENICO
 
 
ChiCTR-INR-16008283: Clinical trial of foscarnet and ganciclovir for prevention of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation

Recruiting
N/A
252
 
Receive foscarnet for prevention of cytomegalovirus infection from engraftment to day+60 after transplantation ;Receive ganciclovir for prevention of cytomegalovirus infection from engraftment to day+60 after transplantation
Department of hematology, Xinqiao Hospital, Third Military Medical University, Chongqing, China; Department of hematology, Xinqiao Hospital, self-paying
cytomegalovirus infection
 
 
ChiCTR1900021195: A study for precision diagnosing and treatment strategies in difficult-to-treat AIDS cases and HIV-infected patients with highly fatal or highly disabling opportunistic infections

Not yet recruiting
N/A
3650
 
No intervention is taken. ;Induction therapy: fluconazole 800mg/d, PO, for 2 weeks; consolidation therapy: fluconazole 400mg/d, PO, for 8 weeks; maintenance therapy: fluconazole 200mg/day, PO, for 1 year. ;Fluconazole 400mg / day, PO, for 1 year. ;When the initial intracranial pressure≥250mmH2O, according to the patients' will, lumbar puncture and removing CSF should be done by regular. ;When the initial intracranial pressure is ≥ 250 mmH2O, lumbar puncture was given daily to reduce intracranial pressure. The intracranial pressure was measured once every 10ml of released cerebrospinal fluid, until the initial intracranial pressure< 50% of the initial intracranial pressure or the pressure< 200 mmH2 ;When the initial intracranial pressure is ≥250mmH2O, the drainage is given, and the cerebrospinal fluid is continuously drained by the improved drainage device to maintain the daily intracranial pressure <200mmH2O; when the intracranial pressure is <200mmH2O for 2 days or more, Stop drainage. ;Amphotericin B deoxycholate combined with flucytosine. Details: amphotericin B deoxycholate 0.5 - 0.7mg / kg, once a day, intravenous drip; flucytosine, daily 100mg / kg, divided into 4 times, PO. Lumbar puncture, biochemical examination of cerebrospinal fluid, cerebrospinal fluid ink staining and fungal culture were p ;Voriconazole combined with flucytosine. Details: Voriconazole was given orally at the induction dose of 400 mg on the first day, once every 12 hours, 200 mg on the second day, once every 12 hours, and flucytosine at the dose of 100 mg/kg per day, four times a day. Lumbar puncture, biochemical ex ;Amphotericin B deoxycholate combined with fluconazole. Details: Amphotericin B deoxycholate 0.5-0.7 mg/kg, once a day, intravenous drip; fluconazole 800 mg, once a day, intravenous drip. Lumbar puncture, biochemical examination of cerebrospinal fluid, cerebrospinal fluid ink staining and fungal culture were performed according to& ;Amphotericin B deoxycholate combined with voriconazole. Details: Voriconazole was administered orally at the induction dose of 400 mg on the first day, once every 12 hours; the maintenance dose of 200 mg on the next day, once every 12 hours; amphotericin B deoxycholate 0.5-0.7 mg/kg once a day, intravenous& ;Subjects start ART after 2 weeks of treatment for cryptococcosis. ;Subjects start ART after 5 weeks of treatment for cryptococcosis. ;SMZ-TMP 1.44g PO q8h + azithromycin 0.5 g IV qd at least for 6 weeks. ;Sulfamethoxazole,Sulfadiazine and Trimethoprim Tablets 1.44g PO q8h + Clindamycin 600mg IV q8h at least for 6 weeks. ;Subjects start ART within 2 weeks of treatment for Toxoplasma gondii. ;Subjects start ART after 2 weeks of treatment for Toxoplasma gondii. ;TMP-SMZ (TMP 15-20 mg/kg/d, SMX 75-100 mg/kg/d) plus prednisone (40 mg 2 times/day, 5 days; 40 mg 1 times/day, 5 days; 20mg 1 time/day, 11 days), total course of treatment 3-4 weeks ;TMP-SMZ (TMP 15-20mg/kg/d, SMX 75-100 mg/kg/d) plus clindamycin (0.6g clindamycin combine with 100ml saline slow) Instillation, 1 time / 6h) plus prednisone (40mg 2 times / day, 5 days; 40mg 1 time / day, 5 days; 20mg 1 time / day, 11 days), the total course of treatment 3-4 weeks. ;Caspofungin (70 mg once daily, 1 day; 50 mg once daily, 20 days) combine with TMP-SMZ (TMP 15-20 mg/kg/d, SMX 75-100 mg/kg/d) plus prednisone (40 mg twice daily, 5 days; 40 mg once daily, 5 days; 20 mg once daily, 11 days), total course of treatment 3-4 weeks. ;Subjects start ART within 1 weeks of treatment for Pneumocystis jirovecii. ;Subjects start ART after 2 weeks of treatment for Pneumocystis jirovecii. ;Induction therapy: sodium foscarnet 60mg/kg, q8h, infusion time > 2h, 2 weeks of treatment; maintenance treatment: sodium foscarnet 90mg/kg/day, intravenous infusion time > 2 h, treatment for at least 2 weeks. At the same time, dexamethasone 5 mg qd was administered intravenously for 4 weeks. ;induction therapy: sodium foscarnet 60mg/kg, q8h, intravenous infusion time > 2h, 2 weeks of treatment; maintenance treatment: sodium foscarnet 90mg/kg/day, intravenous infusion time > 2 h, treatment for at least 2 weeks . At the same time, combined with ganciclovir 0.2 ~ 0.4mg qw intra-balloon injection for ;induction therapy: sodium foscarnet 60mg/kg, q8h, infusion time > 2h, 2 weeks of treatment; maintenance treatment: sodium foscarnet 90mg/kg/day, intravenous infusion time > 2h, treatment for at least 2 weeks. ;Subjects start ART within 2 weeks of treatment for CMV. ;Subjects start ART after 2 weeks of treatment for CMV. ;The amphotericin B deoxycholate was given intravenously for 2 weeks, the dose was 5 mg on the first day, 15 mg on the second day, and 0.5-0.7 mg/kg/d on the third day and later. Then changed to oral itraconazole capsule 200 mg q12 h for 10 weeks, the total course of treatment for 12 ;Voriconazole 4 mg/kg q12h for 4 days, the first day was given a loading dose (voriconazole 6 mg / kg q12 h). After 4 days, it was changed to oral voriconazole capsule 200 mg q12h. After 2 weeks of voriconazole, it was changed to oral itraconazole 200 mg q12 h for 10 weeks. The total& ;Voriconazole 4 mg/kg q12h for 2 weeks,the first day was given a loading dose (voriconazole 6mg/kg q12h), and then changed to oral voriconazole capsule 200 mg q12h for 10 weeks, the total course of treatment for 12 weeks. ;Subjects start ART within 2 weeks of treatment for Talaromyces marneffei. ;Subjects start ART after 2 weeks of treatment for Talaromyces marneffei.
Chongqing Public health medical center; Chongqing Public health medical center, National Science and Technology Major Project -
AIDS opportunistic infections and refractory AIDS
 
 
ChiCTR2000031933: Foscarnet sodium for the treatment of pure erythrocyte aplastic anemia due to parvovirus B19 infection after kidney transplantation:study protocol for a prospective single-center trial

Not yet recruiting
N/A
20
 
Foscarnet ( IV.)
The First Affiliated Hospital of Zhejiang University School of Medicine; The First Affiliated Hospital,college of medicine,Zhejiang University, Self-funded
Pure red blood cell aplastic anemia after kidney transplant
 
 
ChiCTR2100044197: The efficacy and safety of foscarnet in the management of refractory herpes simplex virus keratitis: a prospective multicentric controlled study

Recruiting
N/A
50
 
Foscarnet ( IV.) ;acyclovir(IV.)
School of Ophthalmology and Optometry and Eye Hospital, Wenzhou Medical University; School of Ophthalmology and Optometry and Eye Hospital, Wenzhou Medical University, National key research and development project
herpes simplex virus keratitis
 
 

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