Clinical Catch-Up: 3's the Charm for Pfizer-BioNTech Vaccine in Kids & More
As Memorial Day officially kicks off the summer season, there are plenty of clinical trial highlights. Here’s a look.
Ocugen reported the FDA had lifted a second clinical hold on its studies of Covaxin, a COVID-19 vaccine. The hold was placed on a Phase II/III trial over concerns about the company’s developmental partner Bharat Biotech International Limited’s manufacturing facility.
Edesa Biotech announced it had initiated enrollment for a second cohort of patients for the Phase III portion of a Phase II/III trial of EB05 for COVID-19-induced Acute Respiratory Distress Syndrome (ARDS). The drug is a monoclonal antibody.
Codagenix dosed the first patient in a Phase I trial of CoviLiv as a booster in healthy adults after previous vaccination with approved COVID-19 vaccines. CoviLiv is an intranasal, live-attenuated virus vaccine.
Armata Pharmaceuticals reported that it had dosed the first patient in its Phase Ib/IIa trial of AP-SA02 for adults with bacteremia from Staphylococcus aureus infections. In June 2020, the company was awarded $15 million from the U.S. Department of Defense through the Medical Technology Enterprise Consortium (MTEC) managed by the Naval Medical Research Center with funding from the Defense Health Agency and Joint Warfighter Medical Research Program, to evaluate AP-SA02 as an adjunct to best available antibiotic treatment.
Alnylam Pharmaceuticals reported 18-month results from a Phase III Helios-A trial of vutrisiran in transthyretin-mediated hereditary (hATTR) amyloidosis. Vutrisiran targets and silences the mRNA linked to the production of TTR proteins. The company also announced new positive results from the Phase III ILLUMINATE-C trial of lumasiran for advanced primary hyperoxaluria type 1 (PH1). The new results were a six-month primary analysis period of the ILLUMINATE-C trial of lumasiran. Lumasiran, marketed as Oxlumo and indicated for primary hyperoxaluria type 1, is an RNAi therapeutic targeting hydroxyacid oxidase 1 (HAO1), the gene encoding glycolate oxidase (GO). The company previously reported that lumasiran caused substantial reductions in plasma oxalate (POx) at six months.
Regeneron Pharmaceuticals reported positive data from its Phase III trial of Evkeeza for homozygous familial hypercholesterolemia (HoFH). Evekeeza (evinacumab) is a fully human monoclonal antibody against ANGPTL3.
Seres Therapeutics reported positive data from the Phase III ECOSPOR trial of SER-109 for the prevention of recurrent C. difficile infection. SER-109 is an oral microbiome therapeutic containing Firmicutes spores, typically found in healthy microbiomes.
Vera Therapeutics announced new data from its Phase II trial of atacicept for systemic lupus erythematosus. Atacicept is a recombinant fusion protein.
Day One Biopharmaceuticals dosed the first patients in sub-study 2 of FIRELIGHT-1, a Phase Ib/II trial of tovorafenib in combination with pimasertib in adolescent and adult patients with recurrent, progressive, or refractory solid tumors with MAPK pathway aberrations. The drug is an oral, brain-penetrant, highly selective type II pan-RAF kinase inhibitor. Pimasertib is an oral, highly selective small-molecule inhibitor of mitogen-activated protein kinases 1 and 2 (MEK-1/-2).
Albireo presented analysis of its pivotal PEDFIC 1 and PEDFIC 2 studies of Bylavy for progressive familial intrahepatic cholestasis (PFIC). Bylvay is a potent, non-systemic once daily ileal bile acid transport inhibitor approved in the U.S. for pruritus in patients three months of age and older in all types of PFIC.
Vectorious Medical Technologies announced the results of Vector-HF I, a first-in-man study of its V-LAP wireless system for left atrial pressure management of heart failure. The V-LAP system in an implanted heart sensor.
Janssen, a Johnson & Johnson company, published findings from the Phase III COMPASS long-term open-label extension study of Xarelto (rivaroxaban) and Xarelto in combination with acetylsalicylic acid (aspirin). The studies supported the role of dual pathway inhibition with Xarelto and aspirin in patients with coronary artery disease (CAD) and/or peripheral artery disease (PAD).
The company also presented data from the Phase II Galaxi 1 trial of Tremfya (guselkumab) in moderately to severely active Crohn’s disease. The data demonstrated that patients who were intolerant of or had poor responses to conventional therapies achieved highly clinical biomarker response levels of 47.5% to 66.7%.
Seagen announced positive topline results from the pivotal Phase II MOUNTAINEER trial of Tukysa (tucatinib) in combination with trastuzumab in patients with previously treated HER2-positive metastatic colorectal cancer. Tukysa is an oral TKI inhibitor.
Stealth Biotherapeutics announced new data from the Phase II Reclaim-2 trial of elamipretide in geographic atrophy secondary to dry age-related macular degeneration. Elamipretide is designed to ameliorate mitochondrial-based diseases of the eye.
Ascendis Pharma announced that results from Visen Pharmaceuticals’ Phase III trial of TransCon hGH in children with growth hormone deficiency in China demonstrated results consistent with Ascendis’ Phase III trial. The drug is already approved in U.S. and EU for pediatric GHD.
Recce Pharmaceuticals announced that in cohort five of a Phase I trial, R327 demonstrated a good safety and tolerability profile among 10 healthy male subjects. The drug, RECCE 327 is an IV and topical therapy being developed for serious and potentially life-threatening infections from Gram-positive and Gram-negative bacteria.
Pfizer presented detailed results from two pivotal studies that make up the Elevate UC Phase III program of etrasimod for moderately-to-severely active ulcerative colitis (UC). The drug is a once-daily, oral, selective sphingosine 1-phosphate (S1P) receptor modulator. Both studies hit all primary and key secondary endpoints.
Eli Lilly shared results from its Phase III Lucent-2 trial of mirikizumab for ulcerative colitis. Patients who responded to the drug at 12 weeks achieved and maintained statistically superior and clinically meaningful improvements at one year compared to placebo across all primary endpoints of clinical remission and all key secondary endpoints. Mirikizumab is a humanized IgG4 monoclonal antibody that binds to the p19 subunit of interleukin 23.
Imugene and City of Hope dosed the first patient in a Phase I trial of CF33-hNIS (Vaxinia) for metastatic or advanced tumors. The drug is a genetically altered oncolytic virus programmed to infiltrate cancer cells and cause them to burst.
Alpine Immune reported the FDA had removed a partial clinical hold on its NEON-2 trial of davoceticept with Merck’s anti-PD-1 checkpoint inhibitor Keytruda (pembrolizumab) in adults with advanced malignancies. Davoceticept is a first-in-class conditional CD28 costimulator and dual checkpoint inhibitor.
Luxa Biotechnology announced the first patient was transplanted with RPESC-RPE-4W for dry age-related macular degeneration in its Phase I/IIa trial. The therapy is a cell product derived from the retinal pigment epithelium stem cell (RPESC) that is present in the adult human retina.
Cingulate completed enrollment in its formulation study of CTx-2103 for the management of anxiety-related disorders. Results from the trial are expected in July 2022. CTx-2103 contains the active pharmaceutical ingredient buspirone hydrochloride, a non-benzodiazepine medication.
Pharmazz announced positive topline data from its Phase III trial of sovateltide for acute ischemic stroke. The data at 90 days demonstrated mRS (median score reduction) had a significantly greater number of patients with an improvement of 2 or more points on mRS. It produced a statistically significant and clinically meaningful improvement in neurological outcomes in patients 90 days post-treatment.
Endeavor BioMedicines dosed the first patient in an open-label Phase II trial of ENV-101 (taladegib) in patients with advanced solid tumors harboring Patched-1 loss of function mutations. ENV-101 is a Hedgehog signaling inhibitor.
Oncotelic Therapeutics reported the FDA had approved its launch of a Phase II trial of OT-101 with Merck’s checkpoint inhibitor Keytruda in metastatic plural mesothelioma. OT-101 is a TGF-beta inhibitor.
Crinetics Pharmaceuticals announced positive results from the multiple-ascending dose (MAD) portion of a Phase I trial of CRN04894 for Cushing’s disease. The drug is a first-in-class, oral, nonpeptide adrenocorticotropic hormone (ACTH) antagonist.
CytomX Therapeutics dosed the first patient in a Phase I trial of CX-904. The drug is a conditionally activated T-cell-engaging bispecific designed to target EGFR on cancer cells and the CD3 receptor on T-cells within the tumor microenvironment.
SciSparc received Ethics Committee approval in Germany and Israel to run a Phase IIb trial of SCI-110 in patients with Tourette syndrome. The drug is based on cannabinoid pharmaceuticals.
SELLAS Life Sciences Group announced topline data from its Phase I/II trial of galinpepimut-S for WT1(+) r/r platinum-resistant advanced metastatic ovarian cancer. The drug is a Wilms Tumor-1 (WT1)-targeting peptide immunotherapeutic. It is being evaluated with Merck’s anti-PD-1 drug Keytruda.
Laekna Therapeutics dosed the first patients in a Phase Ib/III trial of afuresertib in combination with fulvestrant in HR+/HER2- breast cancer patients who failed after one or two lines of CDK4/6 inhibitors, endocrine, or chemotherapy treatments. Afuresertib in an AKT kinase inhibitor.
Yingli Pharma US dosed the first patient in its Phase I study of YL-13027. The drug is a potent and selective TGF beta receptor 1 inhibitor being developed for advanced solid tumors.
Scioto Biosciences announced topline results from a Phase Ib trial of SB-121 in patients with an autism spectrum disorder. The drug is based on a novel microbiome delivery platform, Activated Bacterial Therapeutics (ABT), which delivers best-in-class, live therapeutic bacteria to the gut. The therapeutic was well tolerated.
Biomind Labs received approval in Argentina to run a third Phase II trial of BMND08 for depression and anxiety in Alzheimer’s disease patients. The drug is a 5-Methoxy-N,N-dimethyltryptamine.
InnoCare Pharma received approval in China to run a Phase II trial of tafasitamab with lenalidomide for r/r diffuse large B-cell lymphoma patients not eligible for autologous stem cell transplantation. Tafasitamab is a humanized Fc-modified cytolytic CD19 targeting monoclonal antibody.
Genentech, a Roche company, announced new data from its glofitamab for r/r diffuse large B-cell lymphoma. The drug is a CD20XCD3 T-cell engaging bispecific antibody. After treatment, 34.9% achieved a complete response, with half achieving an overall response.
Bristol Myers Squib reported positive Phase II data from its study of Breyanzi (lisocabtagene maraleucel) for r/r large B-cell lymphoma after first-line therapy who were not deemed candidates for high-dose chemotherapy or hematopoietic stem cell transplant. Breyanzi is a form of CAR-T therapy.
AstraZeneca announced the first patients had been dosed in the IRIS Phase III trial of Saphnelo (anifrolumab) in lupus nephritis. The drug has been approved for adults with moderate to severe systemic lupus erythematosus who are receiving standard care.
Purple Biotech announced positive interim safety and efficacy data from the Phase I trial of NT219 in adults with advanced solid tumors. The drug is a first-in-class small molecule, a director inhibitor of Insulin Receptor Substrates ½ and STAT3.