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Pipeline
January 10, 2020
Company | Drug/Device | Medical Condition | Status |
---|---|---|---|
X4 Pharmaceuticals | Mavorixafor in Combination with Ibrutinib | Waldenström’s macroglobulinemia | phase 1b clinical trial initiated, enrolling 12 to 18 patients |
Sol-Gel Technologies | SGT-210 | punctate palmoplantar keratoderma type -1 | phase 1 proof-of-concept study initiated, enrolling 15 patients |
BioXcel Therapeutics | BXCL501 (dexmedetomidine) | agitation associated with dementia | phase 1b/2 initiated, enrolling first patient |
Agenus | AGEN1223 | cancer | phase 1 trial initiated, dosing first patient |
InhibRX | INBRX-106 | solid tumors | phase 1 trial initiated, dosing first patient |
Locus Biosciences | LBP-EC01 | e. coli bacteria causing urinary tract infections | phase 1b trial opened for enrollment |
Gemini Therapeutics | GEM103 | dry age-related macular degeneration | phase 1 trial initiated, enrolling 9 patients |
Cytokinetics | CK-3773274 (CK-274) | hypertrophic cardiomyopathy | phase 2 trial opened to enrollment |
Protagonist Therapeutics | hepcidin mimetic PTG-300 | hereditary hemochromatosis | phase 2 initiated |
CStone Pharmaceuticals Blueprint Medicines |
fisogatinib in combination with CS1001 | locally advanced or metastatic hepatocellular carcinoma | phase 1b/2 trial’s dosing of first patient |
Opthea | OPT-302 administered in combination with aflibercept (Eylea®) | diabetic macular edema | phase 2a trial patient recruitment completed for 108 patients |
Galera Therapeutics | avasopasem manganese (GC4419) | radiation-induced esophagitis in patients with lung cancer | phase 2a trial first patient dosed, enrolling 60 patients |
TLC | TLC590 | pain management | part 2 of a phase 2 trial dosing first patient of 150 patients |
PellePharm | patidegib topical gel, 2%, | non-Gorlin High Frequency Basal Cell Carcinoma | phase 2 trial dosing first 2 patients of 40 patients |
Promethera Biosciences | HepaStem | acute-on-chronic liver failure | phase 2b trial initiated, enrolling 363 patients |
Zai Lab Novocure |
Tumor Treating Fields in combination with chemotherapy | gastric adenocarcinoma | phase 2 trial, first patient enrolled of 50 patients |
SELLAS Life Sciences Group | galinpepimut-S | acute myeloid leukemia | phase 3 trial enrolling 116 patients across approximately 50 clinical sites in the U.S. and Europe |
BioXcel Therapeutics | BXCL501 (dexmedetomidine) | agitation associated with schizophrenia and bipolar disorder | phase 3 trial enrolling up to 750 patients 18 to 75 years of age |
Clover Biopharmaceuticals | SCB-808 (etanercept biosimilar) | ankylosing spondylitis | phase 3 trial enrolling patients at multiple sites in China |
Eli Lilly | LOXO-292 (selpercatinib) | RET-mutant medullary thyroid cancer | phase 3 trial enrolling 400 patients |
Mallinckrodt Pharmaceuticals | Acthar Gel (repository corticotropin injection) | severe keratitis | phase 4 trial enrolling 30 patients |
Reflow Medical | Temporary Spur Stent System | below-the-knee peripheral artery disease | Breakthrough Device designation granted by the FDA |
Savara | Molgradex | autoimmune pulmonary alveolar proteinosis | Breakthrough Therapy designation granted by the FDA |
Advaxis | ADXS-504 | prostate cancer | IND approval granted by the FDA |
OncoImmune | ONC-392 | non-small cell lung cancer | IND approval granted by the FDA |
Colospan | CG-100 temporary intraluminal bypass device | anastomotic leaks in patients undergoing colorectal surgery | IDE granted by the FDA |
Merck | Keytruda (pembrolizumab) | Bacillus Calmette-Guerin -unresponsive, high-risk, non-muscle invasive bladder cancer with carcinoma in situ | Approved by the FDA |
Blueprint Medicines | AYVAKIT (avapritinib) | unresectable or metastatic gastrointestinal stromal tumor | Approved by the FDA |
Novo Nordisk | Fiasp (insulin aspart injection) | pediatric diabetes | New indication approved by the FDA |
AstraZeneca Merck |
Lynparza (olaparib) | pancreatic cancer | Approved by the FDA |
Myriad Genetics | BRACAnalysis CDx | metastatic pancreatic cancer with a germline BRCA mutation | Approved by the FDA |
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