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Dr John A (Chip) Scarlett

First-in-class telomerase inhibitor approved for blood cancer

The FDA’s regulatory approval of the telomerase inhibitor is welcome,…

7 June 2024 | By Catherine Eckford (European Pharmaceutical Review)

The FDA’s regulatory approval of the telomerase inhibitor is welcome, considering the high unmet need for many lower-risk myelodysplastic syndromes (LR-MDS) patients, according to Geron.

news

EMA validates MAA for novel telomerase inhibitor

Following European validation of its Marketing Authorisation Application (MAA), imetelstat…

2 October 2023 | By Catherine Eckford (European Pharmaceutical Review)

Following European validation of its Marketing Authorisation Application (MAA), imetelstat has potential to become a standard of care in lower risk myelodysplastic syndromes (MDS), according to Geron’s CEO.

news

First-in-class telomerase inhibitor aids transfusion independence in clinical trial

Telomerase inhibitor imetelstat benefitted both major subtypes of lower risk…

5 January 2023 | By Catherine Eckford (European Pharmaceutical Review)

Telomerase inhibitor imetelstat benefitted both major subtypes of lower risk MDS in a Phase III trial for the first time.

article

The promise of telomerase inhibitors for treating blood cancer

Geron’s CEO Chip Scarlett discusses the company’s leading telomerase inhibitor…

8 December 2022 | By Catherine Eckford (European Pharmaceutical Review)

Geron’s CEO Chip Scarlett discusses the company’s leading telomerase inhibitor in this exclusive interview ahead of the 2022 American Society of Hematology Annual Meeting.

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