Abstract: The present disclosure provides compositions and methods related to the treatment of non-tuberculous mycobacterial infections in a subject. In particular, the present disclosure provides compositions comprising an anti-malarial agent and associated methods of treating and/or preventing a non-tuberculous mycobacterial infection in a subject using the composition.
Abstract: Disclosed are methods for treating a neuromuscular disorder, muscle disorder, heart disease, pulmonary fibrosis, liver disease, inflammatory bowel disease, or cancer. Also disclosed is a method of enhancing cancer immunotherapy.
Type:
Application
Filed:
July 26, 2023
Publication date:
May 2, 2024
Inventors:
Penelope Andreux, Klaus Andreas Dugi, Christopher L. Rinsch, Florian Greten, Dominic Denk
Abstract: Provided are compositions suitable for treating acne, disrupting a biofilm, and/or killing bacteria contained in a biofilm. Certain compositions comprise a. about 0.1 wt. % to about 7.5 wt. % glycolic acid; b. about 0.1 wt. % to about 5 wt. % gluconolactone; c. about 0.1 wt. % to about 5 wt. % mandelic acid d. a glycol; e. a salt-tolerant thickening polymer, wherein the total amount of glycolic acid, gluconolactone and mandelic acid is less than about 15 wt. % of the total composition.
Type:
Application
Filed:
January 12, 2024
Publication date:
May 2, 2024
Inventors:
Aliaksandr Zhuk, Anthony Geonnotti, Dara Miller, Jennifer Li
Abstract: The present invention relates to a composition including decursinol as an active ingredient for preventing or treating angina, arteriosclerosis, cerebral infarction, and hypertension. Poorly soluble decursinol was found to improve angina, arteriosclerosis, cerebral infarction, prostate hypertrophy, and diabetic hypertension by inhibiting the overgrowth of vascular endothelial cells, and is expected to be usable in the development of a composition for preventing or treating angina, arteriosclerosis, cerebral infarction, prostate hypertrophy, and diabetic hypertension.
Type:
Application
Filed:
January 11, 2022
Publication date:
May 2, 2024
Applicant:
KYUNGSUNG UNIVERSITY INDUSTRY COOPERATION FOUNDATION
Inventors:
Jae Seon KANG, Hyung Hoi KIM, Jae Sung PYO, Seong Jae LEE, Ye Jin HWANG, Hyeong Soo KIM, Jae Ki CHOI
Abstract: The present invention provides anti-HBV compounds, pharmaceutically acceptable compounds or stereoisomers thereof, and preparation methods and uses for treating, eradicating or inhibiting HBV infection or for alleviating liver injury caused by HBV infection, and so on.
Type:
Application
Filed:
November 17, 2023
Publication date:
May 2, 2024
Applicant:
XI'AN XINTONG PHARMACEUTICAL RESEARCH CO., LTD.
Abstract: The present invention includes a method of inducing vascular regression in poorly perfused blood vessels in a subject comprising providing the subject with an effective amount of an inhibitor of an Endothelial ETS Family Transcription Factor. The compounds of the present invention are used in the treatment of retinopathy of prematurity (ROP), diabetic retinopathy (DR), or vascular malformations.
Abstract: This disclosure provides methods of reducing the risk of prostate cancer progression in patients with a histologically proven prostate cancer characterized as low or intermediate risk for which no other treatment for prostate cancer is indicated. The method comprises administering enzalutamide as a monotherapy in an amount and for a period of time clinically proven effective in reducing the risk of prostate cancer progression in a control population of patients under active surveillance and having histologically proven prostate cancers characterized as low or intermediate risk for which no other treatment for prostate cancer is indicated.
Abstract: There is provided tinostamustine or a pharmaceutically acceptable salt thereof for use in the treatment of triple negative breast cancer (TNBC) to a patient in need thereof.
Abstract: Disclosed are a combination treating prostate cancer, a pharmaceutical composition and a treatment method. The combination includes one of a benzoheterocyclic compound as shown in formula (I), a pharmaceutically acceptable salt thereof, a solvate thereof, a crystalline form thereof, a co-crystal thereof, a stereoisomer thereof, an isotope compound thereof, a metabolite thereof and a prodrug thereof, and an androgen receptor pathway modulator. The combination, the pharmaceutical composition thereof and the treatment method inhibit prostate cancer in a more effective manner.
Type:
Application
Filed:
January 5, 2024
Publication date:
May 2, 2024
Inventors:
Chuansheng GE, Baisong LIAO, Wen-Cherng LEE
Abstract: Provided herein is a compound and method for treating cancer cells. The method comprises administering cancer cells with a compound having the chemical structure of 2-{4-[4-methoxy-3-(trifluoromethyl)phenyl]-1H-pyrazol-1-yl}-N-(2-methyl-2H-1,2,3-triazol-4-yl)acetamide to induce apoptosis of the cancer cells and inhibit tubulin polymerization.
Type:
Application
Filed:
October 27, 2023
Publication date:
May 2, 2024
Inventors:
Renato J. Aguilera, Edgar A. Borrego Puerta
Abstract: The present disclosure features disclosed method of treating disorders such as COPD, bronchitis and/or asthma using disclosed compounds, optionally together with one or more additional active agents. Contemplated methods include administrating orally or by inhalation to a patient one or more disclosed compounds.
Type:
Application
Filed:
December 15, 2023
Publication date:
May 2, 2024
Inventors:
John Miller, Cecilia M. Bastos, Benito Munoz
Abstract: Compositions and method of the present invention comprise novel formulations for increasing the effectiveness of antiviral agents and for preventing and treating symptoms associated with the common cold and viral infections. The present invention is directed to treating symptoms resulting from viral infections and diseases associated with Picomaviridae, Coronaviridae, Orthomyxoviridae, Paramyxovirinae, Reoviridae, and Adenoviridae. The novel formulations provided herein improve the therapeutic ratio of antiviral agents such as pleconaril.
Abstract: The present invention relates to a pharmaceutical combination comprising a first active ingredient which is (R)-5-[3-chloro-4-(2,3-dihydroxy-propoxy)-benz[Z]ylidene]-2-([Z]propylimino)-3-o-tolyl-thiazolidin-4-one or a pharmaceutically acceptable salt thereof and a second active ingredient which is selected from the group consisting of methyl fumarate, dimethyl fumarate, (N,N-diethylcarbamoyl)methyl methyl (2E)but-2-ene-1,4-dioate, and 2-(2,5-dioxopyrrolidin-1-yl)ethyl methyl (2E)but-2-ene-1,4-dioate, or a pharmaceutically acceptable salt thereof.
Abstract: The present invention relates to a pharmaceutical combination comprising a first active ingredient which is ponesimod and a second active ingredient which is selected from the group consisting of teriflunomide and leflunomide.
Abstract: The invention relates to modulators of Embryonic Ectoderm Development (EED) and/or Polycomb Repressive Complex 2 (PRC2) useful in the treatment of disorders and diseases associated with EEC and PRC2, being macrocyclic azolopyridine derivatives and compositions thereof of Formula I: or a pharmaceutically acceptable salt, prodrug, solvate, hydrate, enantiomer, isomer, or tautomer thereof, wherein X1, X2, X3, A1, A2, Y, R1, R2, R3, and R4 are as described herein.
Type:
Application
Filed:
December 20, 2022
Publication date:
May 2, 2024
Inventors:
Ivan Viktorovich Efremov, Steven Kazmirski, Qingyi Li, Lorin A. Thompson, III, Owen Brendan Wallace, Shawn Donald Johnstone, Feng Zhou, Peter Rahl
Abstract: The invention provides novel pharmaceutical compositions of berberine or a derivative or analog of berberine, or a salt thereof, in combination with one or more omega-3 fatty acids or esters thereof, and methods of their use in treating inflammatory bowel disease.
Abstract: Provided herein is an ophthalmic composition. In some embodiments, the ophthalmic composition comprises a low concentration of an ophthalmic agent for treatment of presbyopia. Further disclosed herein is an ophthalmic composition including a low concentration of an ophthalmic agent and deuterated water.
Type:
Application
Filed:
February 3, 2022
Publication date:
May 2, 2024
Inventors:
Gregory I. OSTROW, Kenneth J. WIDDER, David S. BAKER
Abstract: Disclosed herein is a polypeptide including a pharmaceutical composition for use in prevention or treatment of a disease or a disorder associated with lysosomal storage and an autophagy-misregulation associated disease. Further provided are agents that bind a region of an N-terminal domain of a lysosomal-associated membrane protein 1 (LAMP-1), and methods for treating or preventing development of a disease or a disorder associated with lysosomal storage, polyglucosan accumulation or abnormal glycogen accumulation and autophagy-misregulation in a subject in need thereof.
Abstract: Compositions comprising a mixture of at least two types of particles wherein a) the first type of particles comprise dabigatran etexilate in the form of the free base or in the form of pharmaceutically acceptable salts, polymorphs, solvates or hydrates thereof; and b) the second type of particles comprise at least one pharmaceutically acceptable organic acid, use of said compositions in the reduction of the risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation and/or in the prevention of venous thromboembolic events in adult patients who have undergone elective total hip replacement surgery or total knee replacement surgery and processes for the preparation of said compositions.
Type:
Application
Filed:
July 21, 2023
Publication date:
May 2, 2024
Applicant:
Breckenridge Pharmaceutical, Inc.
Inventors:
Pratibha S. PILGAONKAR, Maharukh T. RUSTOMJEE, Anilkumar S. GANDHI
Abstract: The present disclosure relates to the treatment of agitation caused by noradrenergic hyperarousal in an agitated subject. The present disclosure provides oromucosal dosage forms comprising effective amounts of latrepirdine either alone or in combination with dexmedetomidine or pharmaceutically acceptable salts thereof and one or more pharmaceutically acceptable carriers and/excipients. Methods of their use are also provided. The present disclosure also provides a method of treating depression by administering oromucosally a therapeutically effective amount of dexmedetomidine alone or in combination with latrepirdine.
Type:
Application
Filed:
February 25, 2022
Publication date:
May 2, 2024
Inventors:
Michael DE VIVO, Friso POSTMA, David Christian HANLEY, Vasukumar KAKUMANU, Subhendu SETH, Dinesh Kumar DHULL
Abstract: The present disclosure relates methods for treating skin disorders caused by an immune deficiency with topical formulations comprising ethyl (R)-4-((1-(2-cyanoacetyl)piperidin-3-yl)amino)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (Compound I) or pharmaceutically acceptable derivative thereof. In particular, the topical formulations described herein may be used to treat atopic dermatitis, alopecia areata, or vitiligo.
Type:
Application
Filed:
February 18, 2022
Publication date:
May 2, 2024
Inventors:
Paul CHANGELIAN, David GORDON, Francis IGNATIOUS, Walter SMITH, Steve TUCKER, Neal Stuart WALKER
Abstract: There is described a method of treating migraine in certain subjects suffering from migraine, by administration of a gepant to the subject. Also described is a method of reducing the incidence of migraine in certain subjects suffering from migraine, by administration of a gepant to the subject. Also described are methods for identifying the certain subjects. Other embodiments are also disclosed.
Abstract: Described herein are novel piperidine urea derived compounds and their pharmaceutical compositions for the treatment of cancer as a monotherapy or a combination therapy with chemotherapeutic agents and/or checkpoint inhibitors.
Type:
Application
Filed:
September 29, 2023
Publication date:
May 2, 2024
Applicant:
NeuroPn Therapeutics, Inc.
Inventors:
Ish Khanna, Sivaram Pillarisetti, Hans Marcus Malkmus, Kathrin Christin Kortschak
Abstract: The present invention provides a reproxalap ophthalmic solution, and methods of using the same for treating a disease or disorder such as allergic conjunctivitis.
Type:
Application
Filed:
September 12, 2023
Publication date:
May 2, 2024
Inventors:
David CLARK, Susan MACDONALD, Stephen Gitu MACHATHA, Lise Lund KJEMS
Abstract: The present disclosure provides therapeutic methods of treating a cancer patient with a vinca alkaloide N-oxide and an immune checkpoint inhibitor.
Abstract: A method treats or prevents cachexia by administering a therapeutic or prophylactic agent for cachexia and contains a combination of a ghrelin receptor agonist a compound having a morphinan skeleton, represented by the following compounds, or a pharmacologically acceptable acid addition salt thereof:
Abstract: Disclosed are a method for producing an aripiprazole suspension, wherein the aripiprazole has a mean particle size of 1 to 10 ?m, the method comprising the steps of: (a) combining bulk aripiprazole and a vehicle to form a primary suspension; (b) subjecting the primary suspension to first pulverization using e.g., a high shear pulverizing machine, a dispersion machine that applies shear force to a material to be processed, a colloid mill, an ultrasonic dispersion machine, or a high-pressure jet type emulsifying dispersion machine to form a secondary suspension; and (c) subjecting the secondary suspension to second pulverization using e.g., a high-pressure jet type emulsifying dispersion machine to form a sterile final suspension; and a method for producing a freeze-dried formulation from the aripiprazole suspension.
Abstract: A process of production of trazodone or trazodone hydrochloride that comprises: (a) preparing an organic phase comprising trazodone in at least one organic solvent; (b) preparing an aqueous phase comprising at least one basic compound; (c) mixing said aqueous phase with said organic phase; (d) heating at a temperature of at least 40° C. for at least 30 minutes; (e) recovering said trazodone; and, optionally, (f) treating said trazodone with hydrochloric acid to obtain trazodone hydrochloride. Trazodone or trazodone hydrochloride comprising less than 15 ppm of alkylating substances, and a pharmaceutical composition comprising said trazodone hydrochloride.
Type:
Application
Filed:
January 12, 2024
Publication date:
May 2, 2024
Applicant:
AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.p.A.
Inventors:
Marcello MARCHETTI, Tommaso IACOANGELI, Giovanni Battista CIOTTOLI, Giuseppe BIONDI (Deceased)
Abstract: The present invention provides methods for inducing rapid and significant dilation of a subject's pupils. In certain embodiments, the method comprises upregulating the alpha-1 receptors in the eye of the subject, thereby increasing sensitivity to alpha-1 agonists. In other embodiments, such upregulation is achieved through administration of at least one compound selected from the group consisting of alpha-2 selective agonists and beta adrenoreceptor antagonists for a period of time prior to the intended time of dilation. After inducing the upregulation of alpha-1 receptors through the administration of at least one compound selected from the group consisting of alpha-2 selective agonists and beta adrenoreceptor antagonists, alpha-1 agonists can be administered to induce rapid and strong pupil dilation.
Abstract: The present invention relates to a compound for inhibition of nonsense-mediated mRNA decay (hereinafter referred to as “NMD”) or a pharmaceutically acceptable salt thereof. The present invention aims to prevent or treat NMD-related disease through the NMD-inhibiting compound.
Abstract: The disclosure features macrocyclic compounds, alone and in combination with other therapeutic agents, as well as pharmaceutical compositions and protein complexes thereof, capable of modulating biological processes including RAS and RAS-RAF inhibition, and their uses in the treatment of cancers.
Type:
Application
Filed:
March 16, 2023
Publication date:
May 2, 2024
Inventors:
Meizhong JIN, Nicholas Perl, Anna Kohlmann, Ning Yin, Jason T. Lowe, Jae Young Ahn, Mark Joseph Mulvihill, Elena S. Koltun, Adrian L. Gill
Abstract: Formulations of HDAC6 inhibitors passing through the blood brain barrier in hypothalamus and inhibiting HDAC6 in the arctuate AgRP neurons in the hypothalamus, are effective to cause weight loss in obese individuals. These inhibitors also restore leptin sensitivity in leptin-resistant individuals.
Type:
Application
Filed:
May 26, 2023
Publication date:
May 2, 2024
Inventors:
Umut Ozcan, Ralph Mazitschek, Dongxian Guan
Abstract: The present disclosure provides methods for treating or preventing a fungal infection with one or more arylamide compounds, or pharmaceutically acceptable salts thereof, or compositions comprising the same and an additional anti-fungal agent, and pharmaceutical compositions comprising one or more arylamide compounds and at least one additional anti-fungal agent.
Type:
Application
Filed:
September 22, 2023
Publication date:
May 2, 2024
Inventors:
Gustavo H. Goldman, Thaila Fernanda dos Reis
Abstract: The present invention relates to N6-adenosine-methyltransferase inhibitors and to dual N6-adenosine-methyltransferase E3 ligase binders in cancer treatment.
Abstract: Novel compounds for treating or inhibiting leishmaniasis and other parasitic protozoan diseases are disclosed herein. The compounds bind to Leishmania tubulin, induce parasite microtubule polymerization, stall Leishmania cell division, and have broad antiparasitic activity.
Type:
Application
Filed:
October 19, 2020
Publication date:
May 2, 2024
Inventors:
Dawn M. WETZEL, Imran ULLAH, Laela M. BOOSHEHRI, Joseph READY, Suraksha GAHALAWAT, Bin HU, Yesu ADDEPALLI
Abstract: Disclosed are compounds and compositions that bind to the La-related protein 1 (LARP1). LARP1 has roles as both a repressor of translation and stabilizer of mRNA transcripts, and therefore functions as a molecular switch in cancer biology. LARP1 also upregulates the proliferation of RNA viruses. Accordingly, the compounds and compositions disclosed herein that bind to LARP1 may be used for treating or preventing cancer or viral infections in a subject.
Type:
Application
Filed:
December 14, 2020
Publication date:
May 2, 2024
Inventors:
Jacob D. DURRANT, Andrea Jeanne BERMAN, Kevin Christopher CASSIDY, Roni Marta LAHR
Abstract: The present invention is directed to the combination therapy of cancer with a BRAF inhibitor and a MEK inhibitor, as well as uses and pharmaceutical compositions thereof.
Abstract: The present disclosure relates to compounds of the Formula (I): and pharmaceutically acceptable salts, as kinase modulators, compatible with the Type-II inhibition of kinases.
Abstract: The present disclosure provides methods for treating chronic active antibody-mediated rejection (CAMR), in a subject, comprising administering to the subject a therapeutically effective amount of a BTK inhibitor, particularly (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo-[1,5-a] pyrimidine-3-carboxamide or a pharmaceutically acceptable salt thereof.
Abstract: This invention is in the area of improved combination treatments for a select group of hard-to-treat cancer patients, including, for example, those with advanced/metastatic triple negative breast cancer (TNBC), recurrent or metastatic urothelial cancer (mUC), or a Trop-2 overexpressing cancer such as non-small cell lung cancer (NSCLC), wherein the improved combination includes the use of trilaciclib and sacituzumab govitecan, and provides increased overall survival and/or reduced toxicity.
Type:
Application
Filed:
December 22, 2023
Publication date:
May 2, 2024
Applicant:
G1 Therapeutics, Inc.
Inventors:
Andrew Beelen, Rajesh Kumar Malik, John Seung-Hoon Yi, Curt Douglas Wolfgang
Abstract: Methods of treating cancer, promoting antigen presentation, or increasing CD8+ T cell infiltration in tumors by inhibiting KDMA5 are provided.
Abstract: The present application relates to a pharmaceutical combination comprising a phosphoinositide 3-kinase (PI3K) inhibitor and a second therapeutic agent, wherein the second therapeutic agent is an immune checkpoint inhibitor, a TGF? inhibitor, a bifunctional immune checkpoint/TGF? inhibitors or combinations thereof. The present application also provides a method of treatment comprising administering the combination, and the use of the drug combination for treating tumors.
Abstract: The present disclosure provides a use of a pharmaceutical composition including adenine and/or a pharmaceutically acceptable salt thereof in a manufacture of a medicament for treating diabetic ulcers, and the medicament can effectively accelerate and enhance wound healing of diabetic ulcers and prevent scar formation.
Abstract: Pharmaceutical compositions comprising reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA) and methods of treating sleep apnea comprising administering reboxetine or a pharmaceutically acceptable salt thereof and an MRA are described herein. In some embodiments, the MRA is oxybutynin or (R)-oxybutynin or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
March 3, 2022
Publication date:
May 2, 2024
Inventors:
Lawrence G. MILLER, Ronald FARKAS, Luigi TARANTO-MONTEMURRO