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- Sam Altman is back at Open AI
Sam Altman is back at Open AI
First Ever Gene therapy approved for Two Blood Disorders
Science Park’s Newsletter
A Magazine for Science Since 2006
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Image Source : Reuters
Altman returns as OpenAI's CEO, led by Bret Taylor and Larry Summers on the initial board, aiming for a restructured board with up to nine new directors
Microsoft's backing facilitates Altman's reinstatement, leading to negotiations and averted employee threats to quit.
Altman's dismissal, attributed to board conflicts and communication issues, triggered a swift reversal amid employee discontent.
OpenAI seeks a balance between responsible AI development and investor support, highlighting challenges for AI startups in navigating ethical concerns and financial demands.
Altman's leadership and AI innovations garnered global attention, although internal clashes with the board influenced his dismissal.
His entrepreneurial ambitions, including plans for an AI chip startup and investment courting, added complexity to internal tensions.
The episode reflects Silicon Valley's history of CEO oustings and comebacks, echoing instances involving Steve Jobs and Jack Dorsey.
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Image Source : The business rule
Pocket FM, an audio entertainment startup, nears $80 million in a new funding round led by Lightspeed.
The funding round may value the Indian startup at nearly $800 million, considering Pocket FM's current revenue growth.
The startup's annualized revenue run rate (ARR) exceeds $160 million, showing significant growth from the past year.
Pocket FM expanded into the U.S. and adopted a pay-as-you-go model, proving successful in attracting customers.
Leveraging a freemium model, the platform allows users to pay for preferred content instead of the entire library.
The micro-transaction model introduced in 2022 allows users to purchase coins for additional content beyond the free quota.
Users spend an average of 110+ minutes daily on the platform, showcasing high engagement levels.
Pocket FM and Lightspeed declined to comment, with Entrackr previously reporting some funding details.
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Image Source : ResearchGate
Britain's medicines regulator approves the world's first gene therapy for sickle cell disease, named Casgevy.
Casgevy, developed by Vertex Pharmaceuticals and CRISPR Therapeutics, utilizes CRISPR-based gene-editing technology.
The treatment is authorized for patients with sickle cell disease and thalassemia aged 12 and above.
How it works :
Casgevy works by targeting the problematic gene in a patient's bone marrow stem cells, enabling the production of properly functioning hemoglobin.
The gene therapy involves chemotherapy to make space for new cells and genetic editing techniques to fix the gene in a laboratory.
Patients, after stem cell collection and infusion of altered cells, report positive outcomes, reducing severe pain and eliminating the need for transfusions.
The groundbreaking treatment marks a significant advancement beyond traditional, arduous bone marrow transplants.
Cost Questions ???
The cost of gene therapy treatments raises concerns about accessibility for those who would benefit the most.
Casgevy is under review by the U.S. FDA, with a decision expected next month.
Impact of Sickle Cell Disease
Sickle cell disease affects millions globally, with Casgevy offering a potential curative option.
The gene therapy underscores the transformative potential of CRISPR-based technology in the medical field.