Julie Wang
Researcher and clinical trial collaborator in MDMA-assisted psychotherapy
Data updated
Papers
Trials
Research Footprint
Julie Wang appears in 9 tracked papers (2020–2024), most studied alongside MDMA and Placebo, across PTSD, Depressive Disorders and Anxiety Disorders.
Most-cited paper: MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study (942 citations).
Frequent co-authors: Rick Doblin, Berra Yazar-Klosinski and Amy Emerson.
Background & Research
Julie B. Wang appears as an author on multiple MAPS-affiliated studies of MDMA-assisted psychotherapy, including randomized controlled trials, pooled analyses, and follow-up outcomes in PTSD and related indications. Publicly available author listings place her on papers alongside researchers such as Michael Mithoefer, Amy Emerson, Rick Doblin, and Jennifer M. Mitchell, indicating a substantial role in the clinical research program.
Key Impact
She is a recurring author on major MDMA-assisted therapy studies, including Phase 2/3 PTSD trials and related neuroimaging and subgroup analyses that have helped establish the clinical evidence base for psychedelic-assisted treatment.
Collaboration Network
22 collaborators· click a node to visit their profile
Full network →Compounds
Topics
Top Collaborators
Affiliations
Institutions, companies, and organisations Julie Wang is associated with.
Resilient Pharmaceuticals
biotechResilient Pharmaceuticals (formerly Lykos Therapeutics, formerly MAPS PBC) is a US-based public benefit corporation developing MDMA-assisted therapy for PTSD. It was founded in 2014 by MAPS as a commercial spinout to carry MAPS MDMA research through late-stage trials and regulatory approval. After two Phase 3 trials and an NDA filing, FDA issued a Complete Response Letter in August 2024 and requested an additional Phase 3 trial before approval. The company subsequently restructured and rebranded, while the public Lykos web presence continues to describe the organisation as pursuing FDA approval for MDMA-assisted therapy. As of the June 2026 review, no public company announcement of a new pivotal trial start or NDA resubmission date was found. VA/DoD-backed MDMA/PTSD research is proceeding in the broader field, but it should not be treated as direct support for Resilient/Lykos NDA resubmission unless linked by company or FDA evidence.
View stakeholder →MAPS
nonprofitMAPS, the Multidisciplinary Association for Psychedelic Studies, is a U.S.-based 501(c)(3) nonprofit research and educational organization founded in 1986. It works nationally and with a broader global audience to develop medical, legal, and cultural contexts for the careful use of psychedelics and marijuana. Its core activities include research, education, advocacy, and convening the field through large public events. In psychedelic medicine and policy, MAPS positions itself as an advocate for legal access, drug policy reform, harm reduction, and health equity. Its Policy & Advocacy work includes legislative advocacy, community organizing, and impact litigation, and it has also launched work on access for system-impacted people and broader health equity in the legal psychedelic ecosystem. Current documented initiatives include the Psychedelic Science conference series, the Health Equity Program, The Zendo Project, and Ask MAPS, which handles public inquiries about therapy, research, and policy reform.
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