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Alzamend Neuro(ALZN) - 2022 Q2 - Quarterly Report
ALZNAlzamend Neuro(ALZN)2021-12-12 16:00

Financial Performance - Research and development expenses for the three months ended October 31, 2021, were 1,750,050,a2681,750,050, a 268% increase from 474,913 in the same period of 2020[127] - General and administrative expenses for the three months ended October 31, 2021, were 1,833,884,a1231,833,884, a 123% increase from 823,033 in the same period of 2020[127] - Total operating expenses for the three months ended October 31, 2021, were 3,583,934,comparedto3,583,934, compared to 1,297,946 for the same period in 2020, reflecting a significant increase[127] - The net loss for the three months ended October 31, 2021, was 3,599,929,comparedtoanetlossof3,599,929, compared to a net loss of 1,354,097 for the same period in 2020, representing a 166% increase[127] - The basic and diluted net loss per common share for the three months ended October 31, 2021, was (0.04),comparedto(0.04), compared to (0.02) for the same period in 2020[127] - Total operating expenses for the six months ended October 31, 2021, were 5.9million,asignificantincreasefrom5.9 million, a significant increase from 2.6 million in the same period of 2020[146] - General and administrative expenses for the six months ended October 31, 2021, were 3.2million,a763.2 million, a 76% increase from 1.8 million in the prior year[148] - The company recorded a net loss of 5.9millionforthesixmonthsendedOctober31,2021,comparedtoanetlossof5.9 million for the six months ended October 31, 2021, compared to a net loss of 2.7 million in the same period of 2020, representing a 122% increase in losses[146] - The company reported a net loss of 5.9millionforthesixmonthsendedOctober31,2021,comparedtoanetlossof5.9 million for the six months ended October 31, 2021, compared to a net loss of 2.7 million for the same period in 2020[161] - The company expects to continue incurring losses for the foreseeable future and needs to raise additional capital until it can generate sufficient revenues[164] Revenue Generation - The company did not generate any revenues during the three months ended October 31, 2021, and does not anticipate generating revenue for the foreseeable future[129] - The company did not generate any revenue during the six months ended October 31, 2021, and does not anticipate generating revenue in the foreseeable future[147] Research and Development - The company submitted an Investigational New Drug (IND) application for AL001 to the FDA on June 30, 2021, and received a "Study May Proceed" letter on July 28, 2021[119] - The Phase I relative bioavailability study for AL001 began in September 2021, with topline data expected in mid to late December 2021[121] - The company has an additional preclinical candidate, AL002, which has transitioned to an extensive program of preclinical study and evaluation[122] - The FDA has agreed to a combined Phase 1/2 study for AL002, with the IND filing now expected in the second quarter of 2022[124] - Research and development expenses for the six months ended October 31, 2021, totaled 2.7million,a2402.7 million, a 240% increase from 784,000 in the same period of 2020[155] - The company incurred interest expense of 30,000forthesixmonthsendedOctober31,2021,relatedtoaconvertiblepromissorynote[160]ThecompanyexperienceddelaysindrugdevelopmentandmanufacturingactivitiesduetoCOVID19,impactingclinicalprotocoldevelopment[173]ThePhaseIrelativebioavailabilitystudyforAL001commencedonSeptember10,2021,todeterminesafedosingforfuturestudies[163]ExpensesStockcompensationexpenseforthethreemonthsendedOctober31,2021,was30,000 for the six months ended October 31, 2021, related to a convertible promissory note[160] - The company experienced delays in drug development and manufacturing activities due to COVID-19, impacting clinical protocol development[173] - The Phase I relative bioavailability study for AL001 commenced on September 10, 2021, to determine safe dosing for future studies[163] Expenses - Stock compensation expense for the three months ended October 31, 2021, was 1.2 million, a 114% increase from 547,000inthesameperiodof2020[132]ProfessionalfeesforthethreemonthsendedOctober31,2021,were547,000 in the same period of 2020[132] - Professional fees for the three months ended October 31, 2021, were 232,000, up 40% from 166,000intheprioryear[133]ResearchanddevelopmentstockcompensationexpenseforthethreemonthsendedOctober31,2021,was166,000 in the prior year[133] - Research and development stock compensation expense for the three months ended October 31, 2021, was 111,000, a 410% increase from 22,000inthesameperiodof2020[142]TotalgeneralandadministrativeexpensesforthesixmonthsendedOctober31,2021,included22,000 in the same period of 2020[142] - Total general and administrative expenses for the six months ended October 31, 2021, included 1.8 million in stock compensation expense, a 58% increase from 1.1millioninthesameperiodof2020[149]Professionalfeesincreasedby1971.1 million in the same period of 2020[149] - Professional fees increased by 197% to 2.1 million in the six months ended October 31, 2021, compared to 710,000in2020,primarilyduetocostsassociatedwiththePhaseIrelativebioavailabilitystudyforAL001[157]CashandFinancingAsofOctober31,2021,thecompanyhadcashof710,000 in 2020, primarily due to costs associated with the Phase I relative bioavailability study for AL001[157] Cash and Financing - As of October 31, 2021, the company had cash of 13.6 million and an accumulated deficit of 22.8million[161]Netcashprovidedbyfinancingactivitieswas22.8 million[161] - Net cash provided by financing activities was 14.9 million for the six months ended October 31, 2021, primarily from the IPO proceeds of approximately 12.9million[171]LicensingandRoyaltiesThecompanyhasaccrued12.9 million[171] Licensing and Royalties - The company has accrued 65,000 in license fees related to the IND application submitted on June 30, 2021, and 190,000forthefirstdosingofpatientsinthePhaseIstudyforAL001[158]Thecompanyhasmilestonepaymentstotaling190,000 for the first dosing of patients in the Phase I study for AL001[158] - The company has milestone payments totaling 9,600,000 related to the AL001 license agreements, with specific due dates tied to clinical trial events[181] - A royalty payment of 3% is required for License 18110, while License 1811 requires a 1.5% royalty on net sales of products developed from the licensed technology[181] Accounting and Reporting - The company does not have any off-balance sheet arrangements that materially affect its financial condition or operations[182] - Recent accounting standards may impact the company's financial statements, as detailed in Note 3 of the Notes to Unaudited Condensed Financial Statements[183] - The company is classified as a smaller reporting company, which exempts it from certain market risk disclosures[185]