August 16, 2021 04:59 PM EDTUpdated August 20, 12:43 PM

After the long, grueling path to EUA, Roche says there is a supply shortage of Actemra

Josh Sullivan

Roche’s drug Actemra was granted emergency use authorization by the FDA for Covid-19 despite some mixed data, but an 11,000-patient analysis soon showed it cut …

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After the long, grueling path to EUA, Roche says there is a supply shortage of Actemra

Josh Sullivan

Sign up to read this article for free.

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Af­ter the long, gru­el­ing path to EUA, Roche says there is a sup­ply short­age of Actem­ra

Josh Sullivan

Sign up to read this article for free.

Among phar­ma CEOs, the IRA now and the IRA lat­er get very dif­fer­ent re­ac­tions

Bris­tol My­ers restarts ra­dio­phar­ma­ceu­ti­cal Phase 3 tri­al, but de­lays read­out by one year

Up­dat­ed: With cost-cut­ting un­der­way, Bris­tol My­ers rais­es guid­ance, touts Phase 3 win and scraps an­oth­er

An­drew Left, short sell­er who cam­paigned against Valeant, is ac­cused of fraud by SEC

Eu­ro­pean drug reg­u­la­tor re­jects Alzheimer's drug Leqem­bi, cit­ing safe­ty con­cerns

Crit­i­cal Junc­tures in Gene Ther­a­py Clin­i­cal Ma­te­r­i­al Man­u­fac­tur­ing: Where Do I Start? And Will It Work?

After the long, grueling path to EUA, Roche says there is a supply shortage of Actemra

Among pharma CEOs, the IRA now and the IRA later get very different reactions

Bristol Myers restarts radiopharmaceutical Phase 3 trial, but delays readout by one year

Updated: With cost-cutting underway, Bristol Myers raises guidance, touts Phase 3 win and scraps another

Andrew Left, short seller who campaigned against Valeant, is accused of fraud by SEC

European drug regulator rejects Alzheimer's drug Leqembi, citing safety concerns

Critical Junctures in Gene Therapy Clinical Material Manufacturing: Where Do I Start? And Will It Work?