Abstract: This disclosure relates to methods and compositions for treating cancer by administering opioid growth factor receptor (OGFR) antagonists. In particular, the present disclosure relates to methods of administering OGFR antagonists locally to the site of cancer cells in the patient diagnosed with cancer.
Abstract: Pharmaceutical compositions and methods of treating or preventing interstitial cystitis of the bladder or the symptoms thereof in a patient that includes administering an H1 receptor antagonist and an H2 receptor antagonist to the patient.
Type:
Application
Filed:
September 21, 2022
Publication date:
August 22, 2024
Inventors:
Reed B. Hogan, II, Thomas P. Dooley, Douglas R. Paul
Abstract: An object of the present invention is to provide a sustained-release injectable preparation which is in a medication administration form that can provide the effect of 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-1H-quinolin-2-one for a prolonged period of time, the preparation releasing a therapeutically effective amount of 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-1H-quinolin-2-one for at least one week. The present invention provides an injectable preparation containing 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-1H-quinolin-2-one or a salt thereof as an active ingredient, which releases the active ingredient in such a manner that its blood concentration is maintained for at least one week.
Abstract: This invention relates to a tablet containing, as an active ingredient, 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-1H-quinolin-2-one or a salt thereof, that has excellent disintegration ability, storage stability and photostability. The tablet of the present invention comprising an uncoated tablet containing 7-[4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butoxy]-1H-quinolin-2-one or a salt thereof as an active ingredient, excipients such as lactose, corn starch, and microcrystalline cellulose; disintegrants such as low-substituted hydroxypropylcellulose, croscarmellose sodium, and sodium carboxymethyl starch; binders such as hydroxypropylcellulose; lubricants such as stearate; and further comprising a coating layer containing hypromellose; talc; titanium oxide; colorant; and the like, the coating layer being applied to the surface of the uncoated tablet.
Abstract: The invention generally relates to compositions for inducing vasoconstriction. The compositions comprise highly selective alpha-2 adrenergic receptor agonists, at low concentrations, such as below 0.05% weight by volume. The compositions preferably comprise brimonidine. The compositions preferably have pH from about 4.0 to about 7.5.
Abstract: The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt or ester thereof, for use in the treatment of cancers. The present invention also relates to a compound of formula I or a pharmaceutically acceptable salt or ester thereof, for use in the treatment of cancer at certain dosage regimens.
Type:
Application
Filed:
May 19, 2022
Publication date:
August 22, 2024
Inventors:
Carmen Kahatt, Pilar Lardelli, Cristian Fernandez, Arturo Soto
Abstract: The present disclosure related to compounds that can be useful as inhibitors of PD-1, PD-L1 or the PD-1/PD-L1 interaction. Also disclosed herein are pharmaceutical compositions of that can include a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and uses of or methods of using a compound of Formula (I), or a pharmaceutically acceptable salt thereof, for the treatment of PD-L1 related diseases including but not limited to liver diseases, cancer, hepatocellular carcinoma, viral diseases, or hepatitis B.
Type:
Application
Filed:
January 17, 2024
Publication date:
August 22, 2024
Inventors:
Tongfei Wu, Pierre Jean-Marie Bernard Raboisson, Francois Gonzalvez
Abstract: The present invention concerns an Axl inhibitor and one or more immune checkpoint (activity) modulators and/or one or more oncolytic viruses, for use in the prevention, treatment or management of cancer, wherein the Axl inhibitor and the one or more immune checkpoint (activity) modulators and/or the one or more oncolytic viruses are administered concurrently, separately or sequentially; compositions containing such components in combination; and methods of treating cancer in a patient by administering such components in combination.
Abstract: The present disclosure relates to the field of medical technology, particularly relates to use of [1,2,4]triazolo [4,3-B]pyridazine derivatives for preventing and treating senescence and senescence-related diseases. In particular, the present disclosure finds that C1632 has significant anti-senescence, anti-fibrosis and anti-vascular calcification effects. C1632 is a known small molecule drug which can be dissolved in water, ethanol or DMSO, it has good thermal stability, low cytotoxicity, good safety profile, good pharmacokinetic properties, and can be flexibly administered in a variety of ways comprising oral administration, intraperitoneal injection, intramuscular injection and intravenous injection. C1632 can be used as a safe, effective and convenient candidate drug.
Type:
Application
Filed:
November 29, 2023
Publication date:
August 22, 2024
Applicant:
The Eighth Affiliated Hospital, Sun Yat-Sen University
Abstract: Embodiments relate to compositions and methods for the treatment of hair loss, which can include treatment of alopecia, via an application of a composition including an alkalizing agent and/or a sulfotransferase enzyme. The composition can be formulated to be an orally administered composition. In some embodiments, the composition is used to increase the response of minoxidil.
Abstract: A pharmaceutical composition for the treatment of cancer and a use thereof are provided. The pharmaceutical composition consists of an FAK inhibitor and a CD44 inhibitor. Also provided is a drug combination of an FAK inhibitor and a CD44 inhibitor for the treatment of cancer. The CD44 inhibitor and FAK inhibitor drug combination can have synergistic effects, significantly improving tumor inhibition effects, reducing toxic side effects, and overcoming tumor drug resistance.
Abstract: The present invention aims at therapeutics to treat and/or prevent Rett syndrome (RTT), autism spectrum disorders or schizophrenia for which no curative therapy has yet been found. The invention relates to pharmaceutical compositions for preventing or treating Rett syndrome (RTT), autism spectrum disorders, or schizophrenia, which comprises a reverse transcription inhibitor for retrotransposon L1.
Type:
Application
Filed:
June 13, 2020
Publication date:
August 22, 2024
Applicants:
KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION, THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Abstract: The present invention relates to novel combination therapies for the treatment of proliferative disorders, such as, for example, cancer. The combination therapies comprises the administration of a METTL3 inhibitor in combination with (i) an immune oncology agent or therapy; (ii) a BCL2 inhibitor, or a pharmaceutically acceptable salt thereof; (iii) an anthracycline topoisomerase 2 inhibitor, or a pharmaceutically acceptable salt thereof; (iv) cytarabine, or a pharmaceutically acceptable salt thereof; (v) a hypomethylating agent, or a pharmaceutically acceptable salt thereof; or (vi) a FLT3 inhibitor, or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
June 1, 2022
Publication date:
August 22, 2024
Inventors:
Oliver Lars Rausch, Mark Robert Albertella, Yaara Ofir-Rosenfeld, Lina Vasiliauskaite
Abstract: The present invention includes methods of treating cancer in a patient, the method comprising the steps of: (a) providing or obtaining a sample from a patient; (b) determining at least one of a level or activity of at least one of: T follicular regulatory (TFR), ST2 Treg, highly suppressive Treg, activated Treg, or effector Treg cells in the sample; (c) comparing the at least one level or activity of the T cells in the sample to a level or activity of the T cells in a reference sample, respectively, for a specific tumor type or a healthy subject; and (d) if the patient has the at least one of the high level or activity of the T cells systemically as compared to the reference sample, then administering a cancer therapy to the patient that comprises a modified dosage or administration of a Phosphoinositide 3-kinase (PI3K) inhibitor.
Type:
Application
Filed:
June 3, 2022
Publication date:
August 22, 2024
Inventors:
Pandurangan Vijayanand, Christian Ottensmeier, Simon Eschweiler, Mitchell Kronenberg
Abstract: Ganciclovir (GCV) is a heterocyclic compound containing a purine ring. An application of the GCV in preparation of a medicine for treating allergic rhinitis is provided, in which the GCV is used as an only active component or use the GCV in combination with another medicine. Studies have shown that the GCV can effectively ameliorate symptoms of AR (allergic rhinitis) patients who are ineffective to anti-allergic medicine treatment in clinical and improve their quality of life. It is found from transcriptomics that the GCV regulates the function of nasal mucosal cilium cells, goblet cells and leukocytes. It is also found that the GCV may change immune balance of body by increasing regulatory T cells, thereby alleviating allergic symptoms in vitro peripheral blood mononuclear cells (PBMCs) medicine test.
Abstract: Methods of treating sleep apnea and snoring comprising administering a norepinephrine reuptake inhibitor, optionally in the absence of an antimuscarinic agent, and optionally as a monotherapy, are described herein. Pharmaceutical compositions comprising norepinephrine reuptake inhibitors, such as edivoxetine and viloxazine, are also described.
Type:
Application
Filed:
June 17, 2022
Publication date:
August 22, 2024
Inventors:
Luigi TARANTO-MONTEMURRO, Ronald FARKAS, David P. WHITE, Lawrence G. MILLER
Abstract: The disclosure provides pharmaceutical compositions comprising a stabilized pharmaceutically acceptable salt of apilimod, and one or more pharmaceutically acceptable excipients, and related compositions and methods for their use in treating neurodegenerative diseases or disorders, cancer, and viral infections.
Type:
Application
Filed:
January 11, 2024
Publication date:
August 22, 2024
Inventors:
Keith Fandrick, Paul Beckett, Lawrence S. Melvin, JR., Peter Ronald Young, Joan Edwards
Abstract: The disclosure relates to methods, compounds for use and medicaments for the treatment of cancer comprising administering to a subject in need thereof a first agent in a therapeutically effective amount and one or more second agents each in a therapeutically effective amount. In some embodiments, the first agent comprises an EZH2 inhibitor. In certain embodiments, the first agent is tazemetostat or a pharmaceutically acceptable salt thereof and the methods of the disclosure are used to treat lung cancer, e.g., non-small cell lung cancer.
Type:
Application
Filed:
February 2, 2024
Publication date:
August 22, 2024
Inventors:
Maria Alejandra RAIMONDI, Dorothy BRACH
Abstract: The present invention provides a combination of a substituted heterocyclyl derivative of formula (I) or a pharmaceutically acceptable salt thereof which is a CDK7 inhibitor along with an anti-cancer agent or a prodrug thereof, and a method of treating and/or preventing cancer in a subject, comprising administering to the subject a compound of formula (I) conjointly with the anti-cancer agent.
Type:
Application
Filed:
May 27, 2022
Publication date:
August 22, 2024
Inventors:
LEENA KHARE, Akhil KUMAR, Ramulu PODDUTOORI
Abstract: The present invention relates to aryl- or heteroaryl-substituted benzene compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.
Type:
Application
Filed:
March 15, 2024
Publication date:
August 22, 2024
Inventors:
Kevin W. KUNTZ, Richard CHESWORTH, Kenneth W. DUNCAN, Heike KEILHACK, Natalie WARHOLIC, Christine KLAUS, Sarah K. KNUTSON, Timothy J.N. WIGLE, Masashi SEKI, Suji SHIROTORI, Satoshi KAWANO
Abstract: The present application relates to treatment of myeloproliferative neoplasms using the JAK1/JAK2 inhibitor, ruxolitinib, in combination with a BET protein inhibitor, 2,2,4-trimethyl-8-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)-6-(methylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one, wherein the combination is unexpectedly synergistic.
Abstract: The present invention relates to novel pharmaceutical composition comprising meloxicam for the treatment of acute pain, wherein the composition comprises at least a hydrophilic polymer and one or more alkalizing agents or combinations thereof.
Type:
Application
Filed:
November 3, 2021
Publication date:
August 22, 2024
Inventors:
Pankaj Devidas Patil, Vivekanand Khyamgonde, Ritesh Kakaria, Ashish Jaiswal, Akhilesh Dixit, Santanu Chakraborty, Amit Antarkar, Abhijit Deshmukh, Jeffrey P. Smith
Abstract: The invention provides compounds of Formula (1), or pharmaceutically acceptable salts The compounds, compositions, methods and kits of the invention are useful for the treatment of pain, itch, and neurogenic inflammation.
Type:
Application
Filed:
September 5, 2023
Publication date:
August 22, 2024
Inventors:
Bridget McCarthy Cole, James Lamond Ellis
Abstract: Provided herein are compositions for reducing symptoms of post-traumatic stress disorder. The compositions include a combination of an N-methyl-D-aspartate (NMDA) receptor antagonist and an anti-depression agent.
Abstract: The invention relates to methods for preventing, slowing the progression of, delaying or treating metabolic disorders induced in patients by the treatment with neuroleptic agents comprising administering to the patients an SGLT2 inhibitor.
Abstract: The present invention relates to compounds, compositions, and methods, for treating viral infections. In particular, entry inhibitor compounds are disclosed for treatment of coronavirus infections, including SARS-COV-1 and SARS-COV-2 infections. The compounds bind to the interface of a SARS-COV-2 spike protein receptor binding domain (RBD) and a host cell ACE-2 receptor. The entry inhibitor compounds show antiviral activity, favorable kinetics, and temporally act at the entry of SARS-COV-2 infection. In embodiments, the compounds are used as medicaments for the inhibition of viral replication including SARS-COV-1 and/or SARS-COV-2 replication, for the treatment or prophylaxis of viral infections including SARS-COV-1 and SARS-COV-2 infections, and/or for the treatment or prophylaxis of an illness due to SARS-COV-1 and SARS-COV-2 infections.
Abstract: The present invention relates to certain cortexolone derivatives of formula (I) and the use of the same as antitumor active ingredients for the curative or adjuvant, or neoadjuvant or palliative treatment of precancerous lesions, dysplasias, metaplasias and tumor diseases, including malignant neoplasias and metastasis. The present invention also relates to pharmaceutical compositions comprising cortexolone derivatives of formula (I) as active ingredients and at least one physiologically acceptable excipient, and to the use of the pharmaceutical compositions as antitumor medicinal products.
Abstract: The present application relates generally to compositions and methods for treating and/or preventing a variety of symptoms and brain-gut disorders related thereto with aminosterols or pharmaceutically acceptable salts or derivatives thereof.
Abstract: Compounds are provided according to Formula (I): Formula (I) and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof; wherein R1, R2, R3, R6, R7, R8, and n are as defined herein. Compounds of the present invention are contemplated useful for the prevention and treatment of a variety of conditions.
Type:
Application
Filed:
March 13, 2024
Publication date:
August 22, 2024
Inventors:
Francesco G. Salituro, Albert Jean Robichaud, Gabriel Martinez Botella
Abstract: The present invention regards a composition comprising lipoic acid, or an acceptable pharmaceutical or food grade salt thereof or a derivative thereof, and a vitamin D, preferably vitamin D3 and/or vitamin D2. Furthermore, the present invention regards said composition for use in a method for the treatment of neurodegenerative diseases and/or for the treatment of peripheral neuropathies.
Abstract: The present disclosure relates to a method of treating Parkinson's Disease and/or Lewy body disease or disorder(s), including Parkinson's disease dementia and dementia with Lewy bodies, comprising administering to a subject ATH-1017.
Type:
Application
Filed:
April 24, 2024
Publication date:
August 22, 2024
Applicant:
Athira Pharma, Inc.
Inventors:
Hans J. Moebius, Xue Hua, Kevin Church, William Walker, Leen H. Kawas
Abstract: Methods for the treatment of a brain injury or a migraine in a mammal including administering a therapeutically effective amount of psilocybin or a pharmaceutically acceptable salt or solvate thereof, to a mammal in need thereof. Use of a pharmaceutical composition including psilocybin or a pharmaceutically acceptable salt or solvate thereof, together with one or more pharmaceutically acceptable carriers, diluents and excipients for the treatment of a brain injury or a migraine in a mammal.
Abstract: A method for treating an infection in a subject is provided. The method includes administering to the subject, via an oral inhalation route, an amount of a composition that is effective to inhibit the infection. The composition contains a phosphatidylglycerol such as POPG.
Type:
Application
Filed:
August 26, 2022
Publication date:
August 22, 2024
Inventors:
Ajay Gupta, Luca Serratore, Jack Sorrell, Jasmine Ahad
Abstract: The present invention relates to a compound for the inhibition of the transmission of malaria in humans, a pharmaceutical composition comprising said compound, and a method for the inhibition of the transmission of malaria in humans comprising the administration of said compound.
Type:
Application
Filed:
April 29, 2024
Publication date:
August 22, 2024
Inventors:
Jana Held, Lais Pessanha de Carvalho, Sara Grõger Otero, Peter G. Kremsner
Abstract: The present invention concerns nutritional compositions for infants and young children that are high in oleic acid and low in palmitic acid and comprise galacto-oligosaccharides, in particular including beta1,3?-galactosyllactose. The nutritional compositions are particularly advantageous for improving intestinal barrier function.
Abstract: The present invention provides compositions, systems, kits, and methods for treating a subject with a known or unknown enveloped or non-enveloped viral infection (e.g., an unknown virus, RSV, ADV, SARS-CoV2, CHKV, DENV, HSV-1, HSV-2, EBOV, MARV, ZIKV, or a weaponized virus) by administering or providing a composition comprising a lipid agent selected from: a sulfatide, a sulfatide analog, a ceramide, a lipid moiety comprising a ceramide, a sulfoglycolipid, a sulfogalactolipid, a glycosphingolipid, a seminolipid, or a sphingomyelin. In some embodiments, the compositions reduce lung or systemic inflammation in the subject and/or inhibit viral infection. In certain embodiments, the compositions herein are employed to stop a natural pandemic or a biological attack (e.g., with new or weaponized viruses).
Abstract: The purpose of the present invention is to provide an agent for preventing or ameliorating Alzheimer's disease, said agent being able to effectively suppress the accumulation of amyloid ? proteins using a safe material, which has been used in foods for many years, and improve spontaneous alternation behavior change ratio. Ceramides (in particular, a glucosylceramide originating in Amorphophallus konjac) can effectively suppress the accumulation of amyloid ? proteins and thus enables the prevention or amelioration of Alzheimer's disease.
Abstract: Provided is a translation inhibitor without occupying ribosome resources. The translation inhibitor without occupying ribosome resources shows a good anti-tumor effect and is highly safe, and can be used in preparation of an anti-tumor drug.
Abstract: Disclosed are methods for treating a disease or condition characterized by decreased expression or reduced function of an ion channel, comprising administering to a subject in need thereof a therapeutically effective amount of a pore-forming polyene macrolide or pore-forming derivative thereof. For example, the pore-forming polyene macrolide may be amphotericin B (AmB), nystatin, or natamycin. The methods can be used to treat cystic fibrosis.
Type:
Application
Filed:
January 5, 2024
Publication date:
August 22, 2024
Inventors:
Martin D. Burke, Alexander G. Cioffi, Katrina A. Muraglia, Jennifer Hou, Anthony S. Grillo
Abstract: Use of Cymarin or a structural analog thereof to treat cancer or a combination of cancers, any one of which or all of which are a chemoresistant cancer or chemoresistant cancers or the like. In various examples, a cancer is pancreatic cancer, colon cancer, lung cancer, breast cancer, prostate cancer, or the like, any of which may be a chemoresistant cancer, or any combination thereof. In various examples, Cymarin or a structural analog thereof potentiates a chemotherapeutic agent for the treatment of a chemoresistant cance. In various examples, a composition, which may be a pharmaceutical composition, comprises Cymarin or a structural analog thereof a combination thereof.
Abstract: Pemafibrate, tofogliflozin, or combinations thereof for use in treating human patients with liver diseases, particularly NASH patients suffering from liver stiffness or liver fibrosis, NASH patients with lobular inflammation, NASH patients with elevated LDL-C, and NASH patients with healthy triglyceride levels.
Abstract: Provided is a pharmaceutical solid-in-oil nano-dispersion composition that may include ascorbic acid or a astable derivative thereof, a surfactant coating the ascorbic acid or its derivative and an oil vehicle, wherein the ascorbic acid or its derivative are uniformly dispersed in the solid-in-oil nano-dispersion composition. In addition to that, the present disclosure provides a method of preparing the solid-in-oil nano-dispersion composition and formulations thereof. Also, after administration the S/O nano-dispersion based dosage form to subject, it will improve the corneal epithelial wounds healing.
Type:
Application
Filed:
June 17, 2021
Publication date:
August 22, 2024
Applicant:
THE UNIVERSITY OF JORDAN
Inventors:
Hatim ALKHATIB, Mai JABER, Bahaa Al Din JABER
Abstract: Provided are 13-membered ribosome targeting compounds that can be used to treat genetic diseases, including genetic diseases that are associated with a premature termination codon mutation or other nonsense mutation. The compounds can induce and/or promote readthrough of the premature termination codon mutation. Also provided are pharmaceutical compositions containing the compounds, methods of using the compounds and processes for making the compounds.
Type:
Application
Filed:
May 31, 2022
Publication date:
August 22, 2024
Inventors:
Roger B. Clark, Yoshitaka Ichikawa, Wesley Francis Austin, Shuhao Shi, Wenying Wang, Xiben Li, Ivan T. Jewett
Abstract: The present disclosure discloses compositions comprising maribavir, methods of providing the same, and compositions providing intermediates useful in providing maribavir.
Type:
Application
Filed:
October 11, 2023
Publication date:
August 22, 2024
Inventors:
Jeffrey Scott DePue, Suresh Kumar Tipparaju, Helge Alfred Reisch, Datong Tang, Kishore Ramachandran