Insulin glargine

别名: 甘精胰岛素; 甘精胰岛素 USP标准品; 甘精胰岛素标准品(JP); 甘精胰岛素, 来得时(甘精胰岛素)
目录号: V50051
甘精胰岛素是一种长效胰岛素类似物。
Insulin glargine CAS号: 160337-95-1
产品类别: New3
产品仅用于科学研究,不针对患者销售
规格 价格 库存 数量
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300U
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产品描述
甘精胰岛素是一种长效胰岛素类似物。甘精胰岛素用于研究糖尿病。
生物活性&实验参考方法
参考文献

[1]. Recombinant Glargine Insulin Production Process Using Escherichia coli. J Microbiol Biotechnol. 2016;26(10):1781-1789.

其他信息
A recombinant LONG ACTING INSULIN and HYPOGLYCEMIC AGENT that is used to manage BLOOD GLUCOSE in patients with DIABETES MELLITUS.
See also: Insulin Glargine (annotation moved to); Insulin Glargine Recombinant (annotation moved to).
*注: 文献方法仅供参考, InvivoChem并未独立验证这些方法的准确性
化学信息 & 存储运输条件
分子式
C267H404N72O78S6
分子量
6062.89025999994
精确质量
365.21
CAS号
160337-95-1
PubChem CID
118984454
外观&性状
Colorless to light yellow liquid
密度
1.1±0.1 g/cm3
沸点
584.5±50.0 °C at 760 mmHg
闪点
307.3±30.1 °C
蒸汽压
0.0±1.6 mmHg at 25°C
折射率
1.583
LogP
2.81
tPSA
2590
氢键供体(HBD)数目
85
氢键受体(HBA)数目
92
可旋转键数目(RBC)
191
重原子数目
423
分子复杂度/Complexity
15300
定义原子立体中心数目
53
SMILES
[H]/N=C(/NCCC[C@@H](C(=O)O)NC([C@@H](NC([C@H]([C@H](O)C)NC([C@@H](NC([C@H]1N(C([C@H]([C@H](O)C)NC([C@@H](NC([C@@H](NC([C@@H](NC(CNC([C@@H](NC([C@@H](NC(CNC([C@H]2NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC3=CC=C(O)C=C3)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC3N=CNC=3)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](C(C)C)NC([C@H](CC3=CC=CC=C3)N)=O)=O)CC(=O)N)=O)CCC(=O)N)=O)CC3N=CNC=3)=O)CC(C)C)=O)CSSC[C@@H]3C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CSSC[C@@H](C(N3)=O)NC([C@@H](NC([C@@H](NC([C@H](C(C)C)NC([C@H]([C@H](CC)C)NC(CN)=O)=O)=O)CCC(=O)O)=O)CCC(=O)N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC3=CC=C(O)C=C3)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC3=CC=C(O)C=C3)C(=O)N[C@H](C(NCC(=O)O)=O)CSSC2)=O)[C@H](CC)C)=O)CO)=O)[C@H](O)C)=O)=O)=O)CCC(=O)O)=O)CCCN/C(=N/[H])/N)=O)=O)CC2=CC=CC=C2)=O)CC2=CC=CC=C2)=O)CC2=CC=C(O)C=C2)=O)=O)CCC1)=O)CCCCN)=O)=O)CCCN/C(=N/[H])/N)=O)\N
InChi Key
COCFEDIXXNGUNL-RFKWWTKHSA-N
InChi Code
InChI=1S/C267H404N72O78S6/c1-29-137(23)212(330-199(355)109-269)260(412)334-211(136(21)22)256(408)305-166(79-86-206(365)366)226(378)298-163(75-82-196(273)352)230(382)326-190-122-421-422-123-191-251(403)322-185(117-341)249(401)312-170(94-129(7)8)234(386)313-176(101-146-57-65-152(346)66-58-146)237(389)299-161(73-80-194(271)350)227(379)308-169(93-128(5)6)232(384)301-165(78-85-205(363)364)229(381)320-182(107-197(274)353)244(396)316-178(103-148-61-69-154(348)70-62-148)240(392)325-188(222(374)290-115-207(367)368)120-418-420-121-189(221(373)288-112-200(356)294-160(76-83-203(359)360)225(377)297-157(53-42-88-284-265(276)277)219(371)287-113-201(357)295-174(99-144-48-36-32-37-49-144)236(388)315-175(100-145-50-38-33-39-51-145)239(391)317-179(104-149-63-71-155(349)72-64-149)247(399)338-216(142(28)345)263(415)339-91-45-56-193(339)254(406)302-158(52-40-41-87-268)231(383)336-214(140(26)343)261(413)303-159(54-43-89-285-266(278)279)224(376)306-167(264(416)417)55-44-90-286-267(280)281)328-258(410)210(135(19)20)333-245(397)172(96-131(11)12)310-238(390)177(102-147-59-67-153(347)68-60-147)314-233(385)168(92-127(3)4)307-217(369)139(25)293-223(375)164(77-84-204(361)362)304-255(407)209(134(17)18)332-246(398)173(97-132(13)14)311-242(394)181(106-151-111-283-126-292-151)319-248(400)184(116-340)296-202(358)114-289-220(372)187(119-419-423-124-192(327-252(190)404)253(405)337-215(141(27)344)262(414)323-186(118-342)250(402)335-213(138(24)30-2)259(411)329-191)324-235(387)171(95-130(9)10)309-241(393)180(105-150-110-282-125-291-150)318-228(380)162(74-81-195(272)351)300-243(395)183(108-198(275)354)321-257(409)208(133(15)16)331-218(370)156(270)98-143-46-34-31-35-47-143/h31-39,46-51,57-72,110-111,125-142,156-193,208-216,340-349H,29-30,40-45,52-56,73-109,112-124,268-270H2,1-28H3,(H2,271,350)(H2,272,351)(H2,273,352)(H2,274,353)(H2,275,354)(H,282,291)(H,283,292)(H,287,371)(H,288,373)(H,289,372)(H,290,374)(H,293,375)(H,294,356)(H,295,357)(H,296,358)(H,297,377)(H,298,378)(H,299,389)(H,300,395)(H,301,384)(H,302,406)(H,303,413)(H,304,407)(H,305,408)(H,306,376)(H,307,369)(H,308,379)(H,309,393)(H,310,390)(H,311,394)(H,312,401)(H,313,386)(H,314,385)(H,315,388)(H,316,396)(H,317,391)(H,318,380)(H,319,400)(H,320,381)(H,321,409)(H,322,403)(H,323,414)(H,324,387)(H,325,392)(H,326,382)(H,327,404)(H,328,410)(H,329,411)(H,330,355)(H,331,370)(H,332,398)(H,333,397)(H,334,412)(H,335,402)(H,336,383)(H,337,405)(H,338,399)(H,359,360)(H,361,362)(H,363,364)(H,365,366)(H,367,368)(H,416,417)(H4,276,277,284)(H4,278,279,285)(H4,280,281,286)/t137-,138-,139-,140+,141+,142+,156-,157-,158-,159-,160-,161-,162-,163-,164-,165-,166-,167-,168-,169-,170-,171-,172-,173-,174-,175-,176-,177-,178-,179-,180-,181-,182-,183-,184-,185-,186-,187-,188-,189-,190-,191-,192-,193-,208-,209-,210-,211-,212-,213-,214-,215-,216-/m0/s1
化学名
(4S)-4-[[2-[[(1R,6R,12S,15S,18S,21S,24S,27S,30S,33S,36S,39S,42R,47R,50S,53S,56S,59S,62S,65S,68S,71S,74R,77S,80S,83S,88R)-88-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S,3S)-2-[(2-aminoacetyl)amino]-3-methylpentanoyl]amino]-3-methylbutanoyl]amino]-4-carboxybutanoyl]amino]-5-oxopentanoyl]amino]-6-[[(2S)-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-amino-3-phenylpropanoyl]amino]-3-methylbutanoyl]amino]-4-oxobutanoyl]amino]-5-oxopentanoyl]amino]-3-(1H-imidazol-4-yl)propanoyl]amino]-4-methylpentanoyl]amino]-53-(2-amino-2-oxoethyl)-62-(3-amino-3-oxopropyl)-77-[(2S)-butan-2-yl]-24,56-bis(2-carboxyethyl)-47-(carboxymethylcarbamoyl)-83-[(1R)-1-hydroxyethyl]-12,71,80-tris(hydroxymethyl)-33,50,65-tris[(4-hydroxyphenyl)methyl]-15-(1H-imidazol-4-ylmethyl)-27-methyl-18,30,36,59,68-pentakis(2-methylpropyl)-7,10,13,16,19,22,25,28,31,34,37,40,49,52,55,58,61,64,67,70,73,76,79,82,85,87-hexacosaoxo-21,39-di(propan-2-yl)-3,4,44,45,90,91-hexathia-8,11,14,17,20,23,26,29,32,35,38,41,48,51,54,57,60,63,66,69,72,75,78,81,84,86-hexacosazabicyclo[72.11.7]dononacontane-42-carbonyl]amino]acetyl]amino]-5-[[(2S)-1-[[2-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S,3R)-1-[(2S)-2-[[(2S)-6-amino-1-[[(2S,3R)-1-[[(2S)-5-carbamimidamido-1-[[(1S)-4-carbamimidamido-1-carboxybutyl]amino]-1-oxopentan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]carbamoyl]pyrrolidin-1-yl]-3-hydroxy-1-oxobutan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-2-oxoethyl]amino]-5-carbamimidamido-1-oxopentan-2-yl]amino]-5-oxopentanoic acid
HS Tariff Code
2934.99.9001
存储方式

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

运输条件
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
溶解度数据
溶解度 (体外实验)
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
溶解度 (体内实验)
注意: 如下所列的是一些常用的体内动物实验溶解配方,主要用于溶解难溶或不溶于水的产品(水溶度<1 mg/mL)。 建议您先取少量样品进行尝试,如该配方可行,再根据实验需求增加样品量。

注射用配方
(IP/IV/IM/SC等)
注射用配方1: DMSO : Tween 80: Saline = 10 : 5 : 85 (如: 100 μL DMSO 50 μL Tween 80 850 μL Saline)
*生理盐水/Saline的制备:将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中,得到澄清溶液。
注射用配方 2: DMSO : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL DMSO 400 μL PEG300 50 μL Tween 80 450 μL Saline)
注射用配方 3: DMSO : Corn oil = 10 : 90 (如: 100 μL DMSO 900 μL Corn oil)
示例: 注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液,加到 900 μL Corn oil/玉米油中, 混合均匀。
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注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如:100 μL DMSO 900 μL (20% SBE-β-CD in Saline)]
*20% SBE-β-CD in Saline的制备(4°C,储存1周):将2g SBE-β-CD (磺丁基-β-环糊精) 溶解于10mL生理盐水中,得到澄清溶液。
注射用配方 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (如: 500 μL 2-Hydroxypropyl-β-cyclodextrin (羟丙基环胡精) 500 μL Saline)
注射用配方 6: DMSO : PEG300 : Castor oil : Saline = 5 : 10 : 20 : 65 (如: 50 μL DMSO 100 μL PEG300 200 μL Castor oil 650 μL Saline)
注射用配方 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (如: 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
注射用配方 8: 溶解于Cremophor/Ethanol (50 : 50), 然后用生理盐水稀释。
注射用配方 9: EtOH : Corn oil = 10 : 90 (如: 100 μL EtOH 900 μL Corn oil)
注射用配方 10: EtOH : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (如: 100 μL EtOH 400 μL PEG300 50 μL Tween 80 450 μL Saline)


口服配方
口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠)
口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素)
示例: 口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中,得到0.5%CMC-Na澄清溶液;然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中,得到悬浮液。
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口服配方 3: 溶解于 PEG400 (聚乙二醇400)
口服配方 4: 悬浮于0.2% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 5: 溶解于0.25% Tween 80 and 0.5% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 6: 做成粉末与食物混合


注意: 以上为较为常见方法,仅供参考, InvivoChem并未独立验证这些配方的准确性。具体溶剂的选择首先应参照文献已报道溶解方法、配方或剂型,对于某些尚未有文献报道溶解方法的化合物,需通过前期实验来确定(建议先取少量样品进行尝试),包括产品的溶解情况、梯度设置、动物的耐受性等。

请根据您的实验动物和给药方式选择适当的溶解配方/方案:
1、请先配制澄清的储备液(如:用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液,按从左到右的顺序依次添加助溶剂,澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明,并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀/澄清;向上述体系中加入50 μL Tween-80,混合均匀/澄清;然后继续加入450 μL ddH2O (或 saline)定容至 1 mL;

3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出,可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果,工作液请现配现用!
6、如不确定怎么将母液配置成体内动物实验的工作液,请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。
制备储备液 1 mg 5 mg 10 mg
1 mM 0.1649 mL 0.8247 mL 1.6494 mL
5 mM 0.0330 mL 0.1649 mL 0.3299 mL
10 mM 0.0165 mL 0.0825 mL 0.1649 mL

1、根据实验需要选择合适的溶剂配制储备液 (母液):对于大多数产品,InvivoChem推荐用DMSO配置母液 (比如:5、10、20mM或者10、20、50 mg/mL浓度),个别水溶性高的产品可直接溶于水。产品在DMSO 、水或其他溶剂中的具体溶解度详见上”溶解度 (体外)”部分;

2、如果您找不到您想要的溶解度信息,或者很难将产品溶解在溶液中,请联系我们;

3、建议使用下列计算器进行相关计算(摩尔浓度计算器、稀释计算器、分子量计算器、重组计算器等);

4、母液配好之后,将其分装到常规用量,并储存在-20°C或-80°C,尽量减少反复冻融循环。

计算器

摩尔浓度计算器可计算特定溶液所需的质量、体积/浓度,具体如下:

  • 计算制备已知体积和浓度的溶液所需的化合物的质量
  • 计算将已知质量的化合物溶解到所需浓度所需的溶液体积
  • 计算特定体积中已知质量的化合物产生的溶液的浓度
使用摩尔浓度计算器计算摩尔浓度的示例如下所示:
假如化合物的分子量为350.26 g/mol,在5mL DMSO中制备10mM储备液所需的化合物的质量是多少?
  • 在分子量(MW)框中输入350.26
  • 在“浓度”框中输入10,然后选择正确的单位(mM)
  • 在“体积”框中输入5,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案17.513 mg出现在“质量”框中。以类似的方式,您可以计算体积和浓度。

稀释计算器可计算如何稀释已知浓度的储备液。例如,可以输入C1、C2和V2来计算V1,具体如下:

制备25毫升25μM溶液需要多少体积的10 mM储备溶液?
使用方程式C1V1=C2V2,其中C1=10mM,C2=25μM,V2=25 ml,V1未知:
  • 在C1框中输入10,然后选择正确的单位(mM)
  • 在C2框中输入25,然后选择正确的单位(μM)
  • 在V2框中输入25,然后选择正确的单位(mL)
  • 单击“计算”按钮
  • 答案62.5μL(0.1 ml)出现在V1框中
g/mol

分子量计算器可计算化合物的分子量 (摩尔质量)和元素组成,具体如下:

注:化学分子式大小写敏感:C12H18N3O4  c12h18n3o4
计算化合物摩尔质量(分子量)的说明:
  • 要计算化合物的分子量 (摩尔质量),请输入化学/分子式,然后单击“计算”按钮。
分子质量、分子量、摩尔质量和摩尔量的定义:
  • 分子质量(或分子量)是一种物质的一个分子的质量,用统一的原子质量单位(u)表示。(1u等于碳-12中一个原子质量的1/12)
  • 摩尔质量(摩尔重量)是一摩尔物质的质量,以g/mol表示。
/

配液计算器可计算将特定质量的产品配成特定浓度所需的溶剂体积 (配液体积)

  • 输入试剂的质量、所需的配液浓度以及正确的单位
  • 单击“计算”按钮
  • 答案显示在体积框中
动物体内实验配方计算器(澄清溶液)
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
第二步:请输入动物体内配方组成(配方适用于不溶/难溶于水的化合物),不同的产品和批次配方组成不同,如对配方有疑问,可先联系我们提供正确的体内实验配方。此外,请注意这只是一个配方计算器,而不是特定产品的确切配方。
+
+
+

计算结果:

工作液浓度 mg/mL;

DMSO母液配制方法 mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL)。如该浓度超过该批次药物DMSO溶解度,请首先与我们联系。

体内配方配制方法μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL ddH2O,混匀澄清。

(1) 请确保溶液澄清之后,再加入下一种溶剂 (助溶剂) 。可利用涡旋、超声或水浴加热等方法助溶;
            (2) 一定要按顺序加入溶剂 (助溶剂) 。

临床试验信息
A Research Study to See How Switching From a Daily Basal Insulin to a New Weekly Insulin, Insulin Icodec, Helps in Reducing the Blood Sugar Compared to Daily Insulin Glargine in Adults With Type 2 Diabetes
CTID: NCT06340854
Phase: Phase 3    Status: Active, not recruiting
Date: 2024-11-19
A Research Study to See How Well New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Levels in People With Type 2 Diabetes (T2D), Compared to Daily Insulin Glargine (COMBINE 4)
CTID: NCT06269107
Phase: Phase 3    Status: Active, not recruiting
Date: 2024-11-19
Efficacy and Safety of SHR-3167 and Insulin Glargine in Type 2 Diabetes Subjects
CTID: NCT06688123
Phase: Phase 2    Status: Not yet recruiting
Date: 2024-11-14
A Research Study to See How Well the New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Level in People With Type 2 Diabetes Compared to Insulin Glargine Taken Daily With Insulin Aspart (COMBINE 3)
CTID: NCT05013229
Phase: Phase 3    Status: Completed
Date: 2024-11-14
A Study of Insulin Efsitora Alfa (LY3209590) Compared to Glargine in Adult Participants With Type 2 Diabetes Who Are Starting Basal Insulin for the First Time (QWINT-1)
CTID: NCT05662332
Phase: Phase 3    Status: Completed
Date: 2024-10-30
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Human Versus Analogue Insulin for Youth With Type 1 Diabetes in Low-Resource Settings
CTID: NCT05614089
Phase: Phase 4    Status: Active, not recruiting
Date: 2024-10-15


A Study of Daily Oral Orforglipron (LY3502970) Compared With Insulin Glargine in Participants With Type 2 Diabetes and Obesity or Overweight at Increased Cardiovascular Risk
CTID: NCT05803421
Phase: Phase 3    Status: Active, not recruiting
Date: 2024-10-09
RCT Glargine vs NPH for Treatment of DM in Pregnancy
CTID: NCT06619301
Phase: Phase 3    Status: Recruiting
Date: 2024-10-01
Effects of Modulators of Gluconeogenesis, Glycogenolysis and Glucokinase Activity
CTID: NCT05098470
Phase: Phase 3    Status: Recruiting
Date: 2024-09-26
Gla-300 and IDeg-100 in Insulin-Naïve People With Type 2 Diabetes Mellitus and Renal Impairment
CTID: NCT05552859
Phase: Phase 4    Status: Terminated
Date: 2024-09-05
A Study of Insulin Efsitora Alfa (LY3209590) as a Weekly Basal Insulin Compared to Insulin Glargine in Adult Participants With Type 2 Diabetes on Multiple Daily Injections
CTID: NCT05462756
Phase: Phase 3    Status: Completed
Date: 2024-08-22
A Research Study to Compare a New Weekly Insulin, Insulin Icodec Used With DoseGuide App, and Daily Insulins in People With Type 2 Diabetes Who Have Not Used Insulin Before
CTID: NCT04760626
Phase: Phase 3    Status: Completed
Date: 2024-08-07
Insulin Degludec vs Insulin Glargine for Glycemic Control in Critical Illness Hyperglycemia
CTID: NCT06178874
Phase: N/A    Status: Completed
Date: 2024-08-05
A Study of LY900014 in Adult Participants With Type 2 Diabetes Mellitus in India
CTID: NCT06370715
Phase: Phase 4    Status: Recruiting
Date: 2024-07-26
A Research Study to Compare Two Types of Insulin, a New Insulin, Insulin Icodec and an Available Insulin, Insulin Glargine, in People With Type 2 Diabetes Who Have Not Used Insulin Before
CTID: NCT04460885
Phase: Phase 3    Status: Completed
Date: 2024-07-05
Early Administration of Insulin Glargine in Patients With Diabetic Ketoacidosis
CTID: NCT06007508
Phase: Phase 2    Status: Terminated
Date: 2024-06-18
Remote And Decentralised Innovative Approaches to Clinical Trials (RADIAL)
CTID: NCT05780151
Phase: Phase 4    Status: Active, not recruiting
Date: 2024-06-12
A Research Study to Compare Two Types of Insulin, a New Weekly Insulin, Insulin Icodec and an Available Daily Insulin, Insulin Glargine, Both in Combination With Mealtime Insulin, in People With Type 2 Diabetes Who Use Daily Insulin and Mealtime Insulin (ONWARDS 4)
CTID: NCT04880850
Phase: Phase 3    Status: Completed
Date: 2024-05-29
Empagliflozin Effect on Glucose Toxicity
CTID: NCT03437330
Phase: Phase 4    Status: Withdrawn
Date: 2024-05-16
Novolog vs. Fiasp Insulin in Non-critically Ill Hospitalized Patients With Type 2 Diabetes Mellitus
CTID: NCT04460326
Phase: Phase 3    Status: Completed
Date: 2024-03-19
Comparison of Glargine to Degludec Insulin Transition With or Without a Bridging Glargine Dose
CTID: NCT04623086
Phase: Phase 4    Status: Completed
Date: 2024-02-28
A Study of Insulin Glargine (LY2963016) in Adult Participants With Type 2 Diabetes in India
CTID: NCT04153981
Phase: Phase 4    Status: Completed
Date: 2024-02-15
A Clinical Study to Compare the Efficacy and Safety of a Novel Medicine (NNC0268-0965) With Insulin Glargine
CTID: NCT04575181
Phase: Phase 1    Status: Completed
Date: 2024-01-10
A Study of LY3209590 in Chinese Participants With Type 2 Diabetes Mellitus
CTID: NCT05596747
Phase: Phase 1    Status: Completed
Date: 2024-01-02
FLuctuATion Reduction With inSULin and Glp-1 Added togetheR (FLAT-SUGAR)
CTID: NCT01524705
Phase: Phase 4    Status: Completed
Date: 2023-12-29
To Compare the Efficacy and Safety of INS068 and Insulin Glargine in Subjects With Type 2 Diabetes Mellitus Not Adequately Controlled With Oral Antidiabetic Drugs
CTID: NCT05699408
Phase: Phase 3    Status: Active, not recruiting
Date: 2023-12-27
Effects of Degludec/Liraglutide on Time in Range, Inflammation and Endothelial Function vs Insulin Basal Bolus in Diabetic Inpatients
CTID: NCT05360537
Phase: Phase 4    Status: Completed
Date: 2023-12-15
Simplified Insulin Regimen for the Elderly
CTID: NCT03660553
Phase: Phase 4    Status: Terminated
Date: 2023-12-12
The Effect of Short-term Insulin Intensive Therapy Based on the Application of Insulin Pump and Real-time Dynamic Glucose Monitoring Technology on Reversing the Newly Diagnosed Type 2 Diabetes
CTID: NCT06127433
Phase: Phase 4    Status: Recruiting
Date: 2023-11-13
The Effect of Exercise on Blood Glucose Levels in Patients With Type 1 Diabetes: A Comparison of 3 Long-acting Insulins
CTID: NCT00313742
Phase: Phase 4    Status: Completed
Date: 2023-11-02
Efficacy and Safety of Dapagliflozin for the Hospital Management of Patients With Type 2 Diabetes
CTID: NCT05457933
Phase: Phase 4    Status: Completed
Date: 2023-10-19
Benefits of Insulin Supplementation for Correction of Hyperglycemia in Patients With Type 2 Diabetes
CTID: NCT02408120
Phase: Phase 4    Status: Completed
Date: 2023-09-28
SITAgliptin Plus GLARgine to Glycemic Control in the Hospital Setting (SITAGLAR-H)
CTID: NCT05579119
Phase: Phase 4    Status: Completed
Date: 2023-09-26
A Research Study of How Overdosing of a New Once Weekly Medicine NNC0148-0287 C (Insulin 287) Influences the Blood Sugar Level in People With Type 2 Diabetes
CTID: NCT03945656
Phase: Phase 1    Status: Completed
Date: 2023-09-06
A Study of Dulaglutide (LY2189265) in Chinese Participants With Type 2 Diabetes
CTID: NCT04591626
Phase: Phase 3    Status: Completed
Date: 2023-05-24
RISE Adult Medication Study
CTID: NCT01779362
Phase: Phase 3    Status: Completed
Date: 2023-05-11
To Compare the Efficacy and Safety of INS068 and Insulin Glargine in Subjects With Type 2 Diabetes Mellitus Treated With Basal Insulin.
CTID: NCT05702073
Phase: Phase 3    Status: Recruiting
Date: 2023-05-09
RISE Pediatric Medication Study
CTID: NCT01779375
Phase: Phase 3    Status: Completed
Date: 2023-04-14
A Clinical Efficacy and Safety Study of Insulin Glargine U300 in Chinese Adult Patients With Uncontrolled Type 2 Diabetes Mellitus With a 3-month Extension Period
CTID: NCT05002933
Phase: Phase 4    Status: Completed
Date: 2023-03-09
A Study of Mealtime Insulin LY900014 in Participants With Type 2 Diabetes Using Continuous Glucose Monitoring (PRONTO-Time in Range)
CTID: NCT04605991
Phase: Phase 3    Status: Completed
Date: 2023-03-03
A Study of LY900014 Compared to Insulin Lispro (Humalog) in Adults With Type 1 Diabetes
CTID: NCT03952130
Phase: Phase 3    Status: Completed
Date: 2023-02-08
Evaluation of the Safety and Efficacy of Insulin Glargine 300 U/ml (Gla-300) in Insulin-naïve Patients With Type 2 Diabetes Mellitus Uncontrolled on Oral Antihyperglycemic Drugs
CTID: NCT04980027
Phase: Phase 4    Status: Completed
Date: 2023-01-31
A Study of Tirzepatide (LY3298176) in Participants With Type 2 Diabetes on Metformin With or Without Sulfonylurea (SURPASS-AP-Combo)
CTID: NCT04093752
Phase: Phase 3    Status: Completed
Date: 2023-01-06
A Study of LY3209590 on Low Blood Sugar in Participants With Type 2 Diabetes Mellitus
CTID: NCT04957914
Phase: Phase 1    Status: Completed
Date: 2022-11-16
Comparison of Glucose Values and Variability Between TOUJEO and TRESIBA During Continuous Glucose Monitoring in Type 1 Diabetes Patients
CTID: NCT04075513
Phase: Phase 4    Status: Completed
Date: 2022-11-14
Comparison of Insulin Degludec With Insulin Glargine U100 for Adults With Type 1 Diabetes Crossing Multiple Time Zones.
CTID: NCT03668808
Phase: Phase 4    Status: Completed
Date: 2022-11-01
A Study to Look at How Safe NNC0472-0147 is in Healthy People and in People With Type 2 Diabetes
CTID: NCT04262661
Phase: Phase 1    Status: Completed
Date: 2022-09-28
Effects of Tirzepatide and Insulin Glargine on Glucolipid Metabolism and Brain Function in Patients With Type 2 Diabetes
CTID: NCT05553093
Phase: Phase 4    Status: Recruiting
Date: 2022-09-23
Efficacy and Safety Of Different Regimens In Patients With Type 2 Diabetes Receiving Intensive Insulin Therapy
CTID: NCT05545800
Phase: Phase 3    Status: Unknown status
Date: 2022-09-19
A Study to Look at How Safe NNC0268-0965 is in People With Type 2 Diabetes
CTID: NCT04136067
Phase: Phase 1    Status: Completed
Date: 2022-09-08
Comparison of Insulin Therapy in Treating Post-Transplant Diabetes
CTID: NCT01963728
Phase: Phase 4    Status: Terminated
Date: 2022-07-26
Comparison of the Efficacy and Safety of Insulin Glargine/Lixisenatide Fixed Ratio Combination to Insulin Glargine in Patients With Type 2 Diabetes Insufficiently Controlled on Basal Insulin
CTID: NCT03798080
Phase: Phase 3    Status: Completed
Date: 2022-07-19
Evaluation of Insulin Glargine/Lixisenatide Fixed Ratio Combination in Patients With Type 2 Diabetes Insufficiently Controlled With Oral Antidiabetic Drug(s)
CTID: NCT03798054
Phase: Phase 3    Status: Completed
Date: 2022-07-19
Outcome of Glargine Insulin in Renal Impairment Patients With Diabetic Ketoacidosis
CTID: NCT05219942
Phase: N/A    Status: Unknown status
Date: 2022-06-07
Early Glargine (Lantus) in DKA Management in Children With Type 1 Diabetes
CTID: NCT03107208
Phase: Phase 4    Status: Completed
Date: 2022-05-10
Comparison of the Efficacy and Safety of a New Formulation of Insulin Glargine With Lantus in Patients With Type 2 Diabetes Insufficiently Controlled With Non-insulin Antidiabetic Therapy
CTID: NCT02855684
Phase: Phase 3    Status: Completed
Date: 2022-04-25
Twelve -Month Study Observing How Insulin-naïve Patients With Type 2 Diabetes Mellitus Manage Diabetes Using Toujeo® After Oral Antidiabetic Drug Failure, the Side Effect of Toujeo®, and The Cost.
CTID: NCT03703869
Phase:    Status: Completed
Date: 2022-04-25
Comparison of Standard vs Higher Starting Dose of Insulin Glargine in Chinese Patients With Type 2 Diabetes (Glargine Starting Dose)
CTID: NCT02836704
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Evaluation of the Efficacy and Safety of Insulin Glargine 300 U/mL in Patients With Type 2 Diabetes Mellitus Uncontrolled on Other Kinds of Insulin
CTID: NCT03760991
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Phase 4 Study to Evaluate Treatment Optimization With Once-daily Insulin Glargine 300 U/mL
CTID: NCT03406000
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Evaluation of Toujeo Insulin in Type 2 Diabetes Patients Inadequately Control With Their Basal Insulin Treatment
CTID: NCT02967237
Phase: Phase 4    Status: Completed
Date: 2022-04-25
A 'Real World' Trial to Determine Efficacy and Health Outcomes of Toujeo Compared to 'Standard of Care' Basal Insulin in Patients Already Using Basal Insulin
CTID: NCT02967211
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination Versus Insulin Glargine in Patients With Type 2 Diabetes (LixiLan-India)
CTID: NCT03529123
Phase: Phase 3    Status: Completed
Date: 2022-04-25
A 'Real World' Trial to Determine Efficacy and Health Outcomes of Toujeo Compared to 'Standard of Care' Basal Insulins in Insulin Naïve Patients Initiating Insulin
CTID: NCT02967224
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Assessment Study of Three Different Fasting Plasma Glucose Targets in Chinese Patients With Type 2 Diabetes Mellitus (BEYOND III/FPG GOAL)
CTID: NCT02545842
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Comparison of Two Treatment Regimens in Patients With Type 2 Diabetes After Short-term Intensive Insulin Therapy
CTID: NCT03359837
Phase: Phase 4    Status: Completed
Date: 2022-04-25
Insulin Degludec and Glargine U100 for Management of Hospitalized and Discharged Patients With Type 2 Diabetes
CTID: NCT03336528
Phase: Phase 4    Status: Completed
Date: 2022-03-31
Efficacy and Safety of Soliqua Versus Lantus in Ethnically/Racially Diverse Patients With Type 2 Diabetes Mellitus Inadequately Controlled on Basal Insulin and Oral Antidiabetic Agents
CTID: NCT03434119
Phase: Phase 3    Status: Terminated
Date: 2022-03-28
Comparison of SAR341402 to NovoLog/NovoRapid in Adult Patients With Diabetes Mellitus Also Using Insulin Glargine
CTID: NCT03211858
Phase: Phase 3    Status: Completed
Date: 2022-03-28
Remission Evaluation of a Metabolic Intervention in Type 2 Diabetes With Sitagliptin (REMIT-Sita)
CTID: NCT02623998
Phase: Phase 3    Status: Completed
Date: 2022-03-25
Comparison of the Safety and Efficacy of HOE901-U300 With Lantus in Children and Adolescents With Type 1 Diabetes Mellitus
CTID: NCT02735044
Phase: Phase 3    Status: Completed
Date: 2022-03-25
A Study of Tirzepatide (LY3298176) Once a Week Versus Insulin Glargine Once a Day in Participants With Type 2 Diabetes and Increased Cardiovascular Risk
CTID: NCT03730662
Phase: Phase 3    Status: Completed
Date: 2022-02-14
A Study of LY900014 Compared to Insulin Lispro (Humalog) in Adults With Type 2 Diabetes
CTID: NCT03952143
Phase: Phase 3    Status: Completed
Date: 2022-02-08
A Study Comparing LY900014 to Insulin Lispro (Humalog) in Children and Adolescents With Type 1 Diabetes
CTID: NCT03740919
Phase: Phase 3    Status: Completed
Date: 2022-01-24
Study for Beinaglutide Versus Glargine Therapy in Glycemic Variability of Type 2 Diabetes Mellitus
CTID: NCT03829891
Phase: N/A    Status: Completed
Date: 2022-01-19
A Trial Comparing the Efficacy and Safety of Insulin Degludec and Insulin Glargine 300 Units/mL in Subjects With Type 2 Diabetes Mellitus Inadequately Treated With Basal Insulin With or Without Oral Antidiabetic Drugs
CTID: NCT03078478
Phase: Phase 3    Status: Completed
Date: 2022-01-11
Impact on the Oxidative Stress of the Different Analogues of Insulin in People With Type 1 Diabetes. (Ineox Study)
CTID: NCT03328845
Phase: Phase 4    Status: Completed
Date: 2021-12-06
Reducing the Risk of Metabolic Decompensation in Diabetic Adolescents by Supervised School Administration of Insulin
CTID: NCT03400501
PhaseEarly Phase 1    Status: Completed
Date: 2021-11-05
Liraglutide Hospital Discharge Trial
CTID: NCT01919489
Phase: Phase 4    Status: Completed
Date: 2021-11-03
Intensive Glycemic Control For Diabetic Foot Ulcer Healing
CTID: NCT04323462
Phase: Phase 4    Status: Unknown status
Date: 2021-11-02
Remission Through Early Monitored Insulin Therapy - Duration Month
CTID: NCT03670641
Phase: Phase 4    Status: Completed
Date: 2021-10-12
Efficacy and Safety of Sotagliflozin Versus Placebo in Participants With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control While Taking Insulin Alone or With Other Oral Antidiabetic Agents
CTID: NCT03285594
Phase: Phase 3    Status: Completed
Date: 2021-05-11
A Research Study to Compare Two Types of Insulin: Insulin 287 and Insulin Glargine in People With Type 2 Diabetes Who Have Not Used Insulin Before
CTID: NCT03951805
Phase: Phase 2    Status: Completed
Date: 2021-04-05
A Research Study to Compare Insulin 287 Once a Week to Insulin Glargine (100 Units/mL) Once a Day in People With Type 2 Diabetes.
CTID: NCT03751657
Phase: Phase 2    Status: Completed
Date: 2021-04-02
Intermediate and Long Acting Insulin Young Children Type 1 Diabetes.
CTID: NCT04664764
Phase: Phase 4    Status: Unknown status
Date: 2021-02-16
A Study to Look at How Safe NNC0268-0965 is in Healthy People and People With Type 1 Diabetes
CTID: NCT03965013
Phase: Phase 1    Status: Completed
Date: 2021-01-14
A Research Study to Compare the Effect of Insulin Degludec and Insulin Glargine on Blood Sugar Levels in People With Type 2 Diabetes - the SWITCH PRO Study
CTID: NCT03687827
Phase: Phase 4    Status: Completed
Date: 2021-01-12
Remission Evaluation of a Metabolic Intervention in Type 2 Diabetes With Forxiga
CTID: NCT02561130
Phase: Phase 4    Status: Completed
Date: 2020-11-24
A Study of Insulin Glargine (LY2963016) in Healthy Chinese Participants
CTID: NCT03555305
Phase: Phase 1    Status: Completed
Date: 2020-11-24
Remission Evaluation of a Metabolic Intervention for Type 2 Diabetes With IGlarLixi
CTID: NCT03130426
Phase: Phase 3    Status: Completed
Date: 2020-11-13
Effect of Insulin Degludec Versus Insulin Glargine on Glycemic Variability in Patients With Type 2 Diabetes Mellitus
CTID: NCT02680457
Phase: Phase 4    Status: Completed
Date: 2020-09-28
Early Administration of Long-acting Insulin Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes
CTID: NCT02548494
Phase: N/A    Status: Terminated
Date: 2020-09-23
Use of NPH Versus Basal Bolus Insulin for Steroid Induced Hyperglycemia
CTID: NCT03511521
Phase: Phase 4    Status: Terminated
Date: 2020-09-11
A Clinical Trial Comparing Glycaemic Control and Safety of Insulin Degludec/Liraglutide (IDegLira) Versus Insulin Glargine (IGlar) as add-on Therapy to SGLT2i in Subjects With Type 2 Diabetes Mellitus
CTID: NCT02773368
Phase: Phase 3    Status: Completed
Date: 2020-08-11
Liraglutide-bolus vs Glargine-bolus Therapy in Overweight/Obese Type 2 Diabetes Patients (LiraGooD)
CTID: NCT03087032
Phase: Phase 4    Status: Unknown status
Date: 2020-08-06
Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination (LixiLan) to Insulin Glargine Alone on Top of Oral Anti-diabetic Drugs (OADs) With Type 2 Diabetes in Japan
CTID: NCT02752828
Phase: Phase 3    Status: Completed
Date: 2020-06-16
Randomised Open Label Study of Insulin Degludec Versus Insulin Glargine U100 in Ramadan
CTID: NCT03349840
Phase: Phase 4    Status: Terminated
Date: 2020-06-09
Remission Evaluation of Metabolic Interventions in Type 2 Diabetes (REMIT Pilot Trial)
CTID: NCT01181674
Phase: Phase 4    Status: Completed
Date: 2020-05-21
A Study of LY900014 in Participants With Type 1 Diabetes
CTID: NCT03214367
Phase: Phase 3    Status: Completed
Date: 2020-05-01
Comparison of the Safety and Efficacy of HOE901-U300 With Lantus in Older Patients With Type2 Diabetes Insufficiently Controlled on Their Current Antidiabetic Medications
CTID: NCT02320721
Phase: Phase 3    Status: Completed
Date: 2020-04-21
A Study of LY900014 Compared to Insulin Lispro in Participants With Type 2 Diabetes
CTID: NCT03214380
Phase: Phase 3    Status: Completed
Date: 2020-03-27
Effects of Local Insulin on Varicose Ulcers for Wound Healing
CTID: NCT04310280
Phase: Phase 3    Status: Completed
Date: 2020-03-17
Sitagliptin for Hyperglycemia in Patients With T2DM Undergoing Cardiac Surgery
CTID: NCT02556918
Phase: Phase 4    Status: Completed
Date: 2019-12-23
A 104 Week Clinical Trial Comparing Long Term Glycaemic Control of Insulin Degludec/Liraglutide (IDegLira) Versus Insulin Glargine Therapy in Subjects With Type 2 Diabetes Mellitus
CTID: NCT02501161
Phase: Phase 3    Status: Completed
Date: 2019-11-27
Single Ascending Dose Study of MK-1092 in Healthy Participants and in Participants With Type 1 and Type 2 Diabetes Mellitus (MK-1092-001)
CTID: NCT03170544
Phase: Phase 1    Status: Completed
Date: 2019-11-15
A 38 Week Trial Comparing Effect and Safety of Insulin Degludec/Insulin Aspart vs. Insulin Glargine Plus Insulin Aspart in Subjects With Type 2 Diabetes Treated With Basal Insulin With or Without Oral Antidiabetic Treatment in Need of Treatment Intensification
CTID: NCT02906917
Phase: Phase 3    Status: Completed
Date: 2019-11-13
Effectiveness of Adding Subcutaneous Long-acting Glargine to Insulin Drip Therapy Compared With Standard Insulin Drip Therapy
CTID: NCT01153100
Phase: Phase 1    Status: Completed
Date: 2019-11-01
Duration of The Honeymoon Phase of Type 1 Diabetes: A Comparison of Insulins Detemir, Glargine and NPH
CTID: NCT00564018
Phase: N/A    Status: Terminated
Date: 2019-10-11
A Comparison of Two Treatment Strategies in Older Participants With Type 2 Diabetes Mellitus (T2DM)
CTID: NCT02072096
Phase: Phase 4    Status: Terminated
Date: 2019-10-09
A Study of Dulaglutide (LY2189265) in Participants With Type II Diabetes
CTID: NCT02152371
Phase: Phase 3    Status: Completed
Date: 2019-09-25
A Study Comparing Dulaglutide With Insulin Glargine on Glycemic Control in Participants With Type 2 Diabetes (T2D) and Moderate or Severe Chronic Kidney Disease (CKD)
CTID: NCT01621178
Phase: Phase 3    Status: Completed
Date: 2019-09-19
A Study to Compare the Effect of a Double Dose of Two Long-acting Insulin Therapies in Participants With Type 2 Diabetes
CTID: NCT02132637
Phase: Phase 3    Status: Completed
Date: 2019-09-18
A Study Comparing the Effects and Safety of Dulaglutide With Insulin Glargine in Type 2 Diabetes Mellitus
CTID: NCT01648582
Phase: Phase 3    Status: Completed
Date: 2019-09-18
Evaluate the Efficacy and Safety of Insulin in Patients With Type 2 Diabetes
CTID: NCT00355849
Phase: Phase 3    Status: Completed
Date: 2019-09-16
A 'Real World' Trial to Determine Efficacy and Health Outcomes of Toujeo (ACHIEVE CONTROL REAL LIFE STUDY PROGRAM)
CTID: NCT02451137
Phase: Phase 4    Status: Completed
Date: 2019-09-10
A Study on Comparison of Glargine Plus Glulisine With Premixed Insulin in Type 2 Diabetes Patients
CTID: NCT02987751
Phase: Phase 4    Status: Completed
Date: 2019-09-10
Exenatide Compared With Insulin Glargine to Change Liver Fat Content in Type 2 Diabetes
CTID: NCT02303730
Phase: Phase 4    Status: Completed
Date: 2019-08-28
A Trial Comparing Cardiovascular Safety of Insulin Degludec Versus Insulin Glargine in Subjects With Type 2 Diabetes at High Risk of Cardiovascular Events
CTID: NCT01959529
Phase: Phase 3    Status: Completed
Date: 2019-07-24
A Study of LY2605541 and Glargine in Participants With Type 1 Diabetes
CTID: NCT01769404
Phase: Phase 1    Status: Completed
Date: 2019-06-24
Exenatide Inpatient Trial: A Randomized Controlled Pilot Trial on the Safety and Efficacy of Exenatide (Byetta®) Therapy for the Inpatient Management of Patients With Type 2 Diabetes
CTID: NCT02455076
Phase: Phase 4    Status: Completed
Date: 2019-06-20
Efficacy and Safety of Semaglutide Once Weekly Versus Insulin Glargine Once Daily as add-on to Metformin With or Without Sulphonylurea in Insulin-naïve Subjects With Type 2 Diabetes
CTID: NCT02128932
Phase: Phase 3    Status: Completed
Date: 2019-06-13
A Trial Comparing the Safety and Efficacy of Insulin Degludec and Insulin Glargine, With or Without OADs in Subjects With Type 2 Diabetes
CTID: NCT02030600
Phase: Phase 3    Status: Completed
Date: 2019-05-10
Comparing Pharmacodynamic and Pharmacokinetic Properties of Insulin Degludec and Insulin Glargine 300 U/mL at Steady-state Conditions in Subjects With Type 1 Diabetes Mellitus
CTID: NCT02536859
Phase: Phase 1    Status: Completed
Date: 2019-05-01
A Study of LY3192767 in Healthy Participants
CTID: NCT03025009
Phase: Phase 1    Status: Completed
Date: 2019-04-05
Multiple Ascending Dose Study of MK-5160 in Participants With Type 1 and Type 2 Diabetes Mellitus (MK-5160-002)
CTID: NCT03095651
Phase: Phase 1    Status: Completed
Date: 2019-04-01
Trial to Compare NNC0123-0000-0338 in a Tablet Formulation and Insulin Glargine in Subjects With Type 2 Diabetes Currently Treated With Oral Antidiabetic Therapy
CTID: NCT02470039
Phase: Phase 2    Status: Completed
Date: 2019-03-18
A Study Comparing Insulin Peglispro With Insulin Glargine as Basal Insulin Treatment
CTID: NCT01894568
Phase: Phase 3    Status: Completed
Date: 2019-03-15
A Study of LY2605541 and Glargine and Exercise in Participants With Type 1 Diabetes
CTID: NCT01784211
Phase: Phase 1    Status: Completed
Date: 2019-03-15
A Study of Insulin Peglispro and Glargine on Fats in Participants With Type 1 Diabetes
CTID: NCT01771250
Phase: Phase 1    Status: Completed
Date: 2019-03-11
A Study to Compare and Measure the Effects of Insulin Peglispro (LY2605541) and Glargine on Meal Time Insulin Requirements
CTID: NCT02152384
Phase: Phase 1    Status: Completed
Date: 2019-03-01
A Study of How Insulin Peglispro (LY2605541) and Insulin Glargine Affect the Breakdown of Fat and Sugar in Type 1 Diabetics
CTID: NCT01925989
Phase: Phase 1    Status: Completed
Date: 2019-03-01
Safety/Efficacy Study of Subcutaneously Injected Prandial Insulins Compared to Insulin Lispro Alone in Participants With Type 1 Diabetes Mellitus
CTID: NCT01194245
Phase: Phase 2    Status: Completed
Date: 2019-02-26
Randomized Sitagliptin Withdrawal Study (MK-0431-845)
CTID: NCT02738879
Phase: Phase 3    Status: Completed
Date: 2019-02-25
Linagliptin Inpatient Trial
CTID: NCT02004366
Phase: Phase 4    Status: Completed
Date: 2019-02-20
A Study to Compare Insulin Intensification of Biphasic Insulin Aspart 30 and Insulin Analogues (Insulin Glargine and Insulin Aspart) in Insulin naïve Type 2 Diabetic Patients
CTID: NCT02453685
Phase: Phase 4    Status: Completed
Date: 2019-02-08
Dulaglutide in Diabetic Patients, Relationship Between Arterial Stiffness, Endothelial Function, Clinical and Laboratory Variables
CTID: NCT03824002
Phase: Phase 4    Status: Completed
Date: 2019-01-31
Efficacy and Safety of FIAsp Compared to Insulin Aspart in Combination With Insulin Glargine and Metformin in Adults With Type 2 Diabetes
CTID: NCT01819129
Phase: Phase 3    Status: Completed
Date: 2019-01-30
Comparison on Efficacy and Safety of Three Inpatient Insulin Therapy in Type2 DM
CTID: NCT01855243
Phase: N/A    Status: Completed
Date: 2019-01-15
A Study to Evaluate the Effectiveness and Safety Initiation and Titration of Insulin Glargine (U300) in Insulin-naïve Patients With Type 2 Diabetes Mellitus (T2DM) Controlled on Oral Antidiabetic Drug Treatment in Turkey
CTID: NCT02954692
Phase: Phase 4    Status: Completed
Date: 2019-01-14
Efficacy of Pramlintide on Prevention of Weight Gain Early Onset of Type 1 Diabetes
CTID: e.querySelector("font strong").i

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